Recalls |
Recalls issued by Food and Drug Administration, Product Safety Commission and National Highway Traffic Safety Administration (NHTSA).For more information on recalls in United States we recommend you visiting Recalls.gov.
ALFA ROMEO ( 13V196000 )
Dated: MAY 13, 2013 Maserati North America, Inc. (Maserati) is recalling certain model year 2005-2008 Quattroporte, 2008 Granturismo, and 2008 Alfa Romeo 8C vehicles. The rear tie rod assemblies may have insufficient an...
CARGO MATE ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
COACHMEN ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
ELGIN ( 13V192000 )
Dated: MAY 06, 2013 Elgin Sweeper Company Inc. (Elgin) is recalling certain model year 2006-2012 Crosswind J Alternative Fuel street sweepers, serial numbers J3285, J3260D, J3261D, J3300D, J3367, J3368D, J3370D, J3385D, ...
EQUIPTER ( 13V191000 )
Dated: MAY 01, 2013 New Heights LLC (New Heights) is recalling certain Equipter RB4000 dump trailers manufactured December 8, 2011, through December 21, 2011. These vehicles are equipped with Carlisle hydraulic brake ac...
FOREST RIVER ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
GULF STREAM ( 13V197000 )
Dated: MAY 09, 2013 Gulf Stream Coach is recalling certain model year 2001 Ultra, Conquest, Independence, Ultra Supreme, Yellowstone, and Cavalier motorhomes with floorplans 6316 or 8325. The motorhomes were manufacture...
MACK ( 13V195000 )
Dated: MAY 10, 2013 Mack Trucks, Inc. is recalling certain model year 2013-2014 CHU, CXU, GU, MRU, and LEU trucks manufactured July 16, 2012, through march 18, 2013 and equipped with drum brakes. The clevis pin for the ...
MAGIC TILT ( 13V188000 )
Dated: MAY 08, 2013 Magic Tilt Trailers is recalling certain boat trailers manufactured October 17, 2011, through January 24, 2012. These trailers are equipped with brake actuators manufactured by Carlisle. On some of t...
MASERATI ( 13V196000 )
Dated: MAY 13, 2013 Maserati North America, Inc. (Maserati) is recalling certain model year 2005-2008 Quattroporte, 2008 Granturismo, and 2008 Alfa Romeo 8C vehicles. The rear tie rod assemblies may have insufficient an...
PALOMINO ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
PRIME TIME ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
SHASTA ( 13V203000 )
Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand...
Pentec Health Announces Limited Voluntary Recall of Certain Compounded Prescription Therapies for Renal Patients
Pentec Health, Inc. has decided to initiate a limited, voluntary recall of in-date nutritional prescriptions for renal patients due to lack of sterility assurance associated with one of its laminar flow hoods used in compounding.
The recall covers renal therapies that were compounded in this hood on or before May 2, 2013.
Tropical Valley Foods Issues Allergy Alert on Undeclared Milk and Walnuts in Next by Nature Dark Chocolate Bananas
Tropical Valley Foods Inc. of Plattsburgh, NY, is recalling next by Nature DARK CHOCOLATE BANANAS, 3 oz. bags, due to undeclared milk and walnuts. People who have an allergy to milk and/or walnuts run the risk of serious or life-threatening allergic reaction if they consume this product.
Rural King Recalls Deer Corn Because of Possible Health Risk
Rural King Distributing of Mattoon, IL is recalling 205 tons of Deer Corn, because it has the potential to be contaminated with aflatoxin. Aflatoxin is a naturally occurring mold by-product.
AUTOCAR ( 13V183000 )
Dated: MAY 08, 2013 Autocar, LLC is recalling certain model year 2012-2013 ACX trucks built May 1, 2012, through November 15, 2012. Due to an insufficient weld, the windshield wiper arms of the vehicles may not be held ...
AUTOCAR ( 13V184000 )
Dated: MAY 08, 2013 Autocar, LLC is recalling certain model year 2005-2013 ACX, WX, and WXLL trucks built November 16, 2004, through September 10, 2012. On the affected vehicles, the air brake systems were built without...
HEARTLAND ( 13V186000 )
Dated: MAY 06, 2013 Heartland Recreational Vehicles (Heartland) is recalling certain model year 2013-2014 Sundance travel trailers, model 322RES, manufactured September 13, 2012, through April 30, 2013. The axles are mo...
KME ( 13V187000 )
Dated: MAY 02, 2013 Kovatch Mobile Equipment Corp. (Kovatch) is recalling certain model year 2009-2013 Predator, Predator SS, Panther; 2010-2011 ARFF; and model year 2010-2013 Panther II emergency vehicles. The grease f...
TEMSA ( 13V185000 )
Dated: MAY 07, 2013 Temsa Global is recalling certain model year 2011-2013 model year TS35C coach buses manufactured from November 2010, through February 2013. Due to a production process error, the fuel tank may develo...
Symbios Medical Products Issues Nationwide Recall of GOPump and GOBlock Kits
May 10, 2013 - Symbios Medical Products initiated a voluntary recall of all GoPump Rapid Recovery System kits and GOBlock Kits manufactured with flow control components assembled prior to July 2012. These products have been found to potentially cause excessively high flow rates, which presents a risk of patient toxicity and serious injury (e.g., seizure, dysrhythmia, death) due to the rapid influx of medication particularly in patients with low body mass or advanced age.
Powell Company Recalls Anywhere Lounger Bean Bag Chairs Due to Suffocation and Strangulation Hazards
Bean bag chairs without a permanent zipper closure allow young children to unzip, ingest or inhale the small beads inside the bean bag chair.
Avon Recalls Microwave Popcorn Maker Due to Burn and Fire Hazards; New Instructions Provided
When cooked too long, the popcorn can overheat in the plastic popcorn maker and ignite.
FLEETWOOD ( 13V189000 )
Dated: APR 26, 2013 Fleetwood RV, Inc. is recalling certain model year 2013 Jamboree Sport Diesel, Providence, Tioga DSL and Tioga Ranger DSL; 2014 Excursion, Expedition, Jamboree Sport, Montara Commercial, Searcher Comm...
Deezo Children?s Hooded Sweatshirts with Drawstrings Recalled by Zulily Due to Strangulation Hazard
The hoodies were sold with drawstrings, which pose a hazard to young children.
Optimus Recalls Portable Electric Heaters Due to Fire Hazard
The portable electric space heater's design can fail to prevent ignition of nearby combustible material.
SUBARU ( 13V194000 )
Dated: MAY 13, 2013 Subaru is recalling certain model year 2013 Outback and Legacy vehicles manufactured from February 15, 2012, through June 15, 2012. In the affected vehicles, the inner and outer shafts of the steerin...
HEARTLAND ( 13V181000 )
Dated: MAY 07, 2013 Heartland Recreational Vehicles is recalling certain model year 2013-2014 Big Country, Bighorn, Elk Ridge, Elk Ridge Express, Landmark, Prowler, Sundance, Sundance XLT, and Silverado fith wheel and tr...
LION ( 13V179000 )
Dated: MAY 06, 2013 Lion Bus, Inc. is recalling one model year 2014 360 bus manufactured in December 2012. Due to insufficient distance between the air compressor discharge line and the hydraulic brake line, the lines m...
SETRA ( 13V190000 )
Dated: APR 23, 2013 Setra Luxury Coaches (Setra) is recalling certain model year 2011 through 2013 Setra S417 TC motorcoaches manufactured between May 2009 and March 2013 and model year 2012 and 2013 S407 motorcoaches ma...
SPARTAN ( 13V182000 )
Dated: MAY 07, 2013 Spartan Motors Chassis (Spartan) is recalling certain model year 2006-2011 K2, and K3 and 2006-2010 MM motorhome chassis manufactured July 20, 2005, through December 17, 2010. The steering gear mount...
TIFFIN ( 13V178000 )
Dated: MAY 02, 2013 Tiffin Motorhomes, Inc. (Tiffin) is recalling certain model year 2013 Breeze and Allegro motorhomes. If the awning installation sequence was not completely followed, the awning motor may unknowingly ...
BRECKENRIDGE ( 13V174000 )
Dated: MAY 06, 2013 Dutchmen Manufacturing is recalling certain model year 2013 Breckenridge recreational vehicles manufactured February 13, 2013, through April 9, 2013. If the awning installation sequence was not compl...
JEEP ( 13V175000 )
Dated: MAY 07, 2013 Chrysler Group LLC (Chrysler) is recalling certain model year 2005-2010 Jeep Grand Cherokee vehicles manufactured February 11, 2004, through March 9, 2010; and 2006-2010 Jeep Commander vehicles manufa...
JEEP ( 13V176000 )
Dated: MAY 07, 2013 Chrysler Group LLC (Chrysler) is recalling certain model year 2008-2012 Jeep Wrangler right-hand drive vehicles manufactured February 1, 2007, through October 10, 2011. The affected vehicles have air...
RAM ( 13V177000 )
Dated: MAY 07, 2013 Chrysler Group LLC (Chrysler) is recalling certain model year 2013 RAM 1500 trucks manufactured manufactured June 25, 2012, through December 12, 2012. In the affected vehicles, the coolant bypass val...
TRIUMPH ( 13V180000 )
Dated: APR 30, 2013 Triumph Motorcycles America, Ltd. is recalling certain model year 2012-2013 Explorer and Explorer XC motorcycles. The Gross Vehicle Weight Rating data on the certification Label is incorrect. Thus, t...
VOLVO BUS ( 13V171000 )
Dated: MAY 01, 2013 Volvo Bus Corporation is recalling certain model year 2009-2013 9700 coaches manufactured from August 28, 2008, through April 19, 2013. Certain conditions may cause the affected coaches to go into a ...
Additional Lots Added: Voluntary Nationwide Recall of 21 Lots of Piperacillin and Tazobactam for Injection, USP 40.5 Grams Due to Possibility of Precipitation / Crystallization in IV Bag or IV Line Upon Reconstitution
May 10, 2013 ? Weston, Florida: Apotex Corp. announced today that it is conducting, on behalf of the manufacturer Hospira, Inc., a voluntary nationwide recall of 21 lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams, NDC number 60505-0773-00 to the hospital / healthcare provider /user level. The impacted lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams may show precipitation / crystallization in IV bag or IV line after reconstitution.
Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients- Expanded to Include SexVoltz 12 Capsules Bottle, SKU 626570615316.
Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU?s 626570609490, 827912089028, 626570617877, 626570615316, 626570615316 Velextra brand SKU?s 626570613855, 626570619055, 626570617860, 626570617563 Amerect SKU?s 626570619031, 626570619628 capsules to the consumer level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. Amerect is voluntarily recalled because it has the potential to contain undeclared tadalafil. Tadalafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the products unapproved new drugs.
Hannaford Supermarkets Issues Allergy Alert for Two Bakery Cookie Products That May Contain Undeclared Nuts
Hannaford Supermarkets is recalling two products sold in the bakery section because they may contain nuts that are not listed on the product packaging label. Individuals who have an allergy or severe sensitivity to any nuts may run the risk of serious or life-threatening allergic reaction should they consume these items.
Smart & Final Expands Recall to Include Additional Production Dates; Allergy Alert - Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini
Smart & Final of Los Angeles, Calif., which previously announced a recall of certain production dates of 2.5 lb - La Romanella Tri-Color Cheese Tortellini, is expanding its recall to include additional production dates due to undeclared wheat, eggs and milk. People who have an allergy or severe sensitivity to wheat, eggs and/or milk run the risk of serious or life-threatening allergic reaction if they consume these products.
In Cooperation with FDA, The Compounding Shop, LLC Declares a Voluntary Recall of All Lots of Sterile Compounded Products Due to a Lack of Sterility Assurance Distributed Within its Local Market Area
The Compounding Shop, LLC is conducting a voluntary recall of all lots of sterile products compounded by the pharmacy that are not expired. The recall is being initiated due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Meijer Recalls Touch Point Baseboard Convection Heaters Due to a Fire Hazard
Touch Point-brand portable electric baseboard convection heaters with a model number of BBC-1500 can overheat.
Krinos Foods, LLC. is Expanding its April 28, 2013 Recall to Include Additional Expiration Dates Jan 01-2014 to Jun 01-2014 of Tahini Products Because of Possible Health Risk
Krinos Foods, LLC. of Long Island City, New York is voluntarily recalling its TAHINI sesame paste, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Dairy Fresh Conducts Voluntary Recall of IGA Brand ?Vanilla & Chocolate? 1.75 Quart Ice Cream Because Package May Contain Undeclared Allergens (Almonds, Coconut, Soy)
Dairy Fresh is voluntarily recalling a specific batch of IGA Brand ?Vanilla & Chocolate? Ice Cream (1.75 quart, 1.66L) with the plant code ?3783? and a SELL BY date of 08-13-13 because it incorrectly contains Heavenly Hash ice cream, which contains almonds, coconut, and soy, which are allergens not declared on the carton. People who have an allergy or severe sensitivity to almonds, coconut, or soy run the risk of serious or life-threatening allergic reaction if they consume this product.
Whole Foods Market Recalls Mislabeled Curried Chicken Salad and Vegan Chick?n Salad Sold at the Cold Salad Bar Due to Undeclared Allergens
May 9, 2013 - CAMBRIDGE, MA. ? Whole Foods Market is recalling bulk curried chicken salad and bulk vegan curried chick'n salad because in some stores these items may have been sold with reversed labels causing undeclared soy and egg allergens. Due to the label mix-up, allergens were undeclared; the vegan chick'n salad contains soy, and the curried chicken salad contains egg.
Pure Herbs Ltd. Issues Allergy Recall Alert on Undeclared Allergens (Milk and Soy) in Protein Extract Urgent Undeclared Allergen Labeling Recall In Pure Herbs Ltd. Protein Extract
Today, Pure Herbs Ltd., Sterling Heights, MI is voluntarily recalling the 4oz and 1oz bottles of Protein Extract because they contain undeclared allergens - milk and soy. This labeling error was discovered during a routine Food and Drug Administration (FDA) inspection when a review of the ingredients found that milk and soy allergen ingredients were not listed on our main label.
Bimeda Inc. on Behalf of Manufacturer Bimeda-MTC Animal Health Inc. Issues Voluntary Nationwide Recall of Sterile Solutions Due to Concerns Regarding Sterility and Possible Health Risk
Bimeda Inc., on behalf of the manufacturer, Bimeda-MTC Animal Health Inc. is voluntarily recalling one lot of Calcium Gluconate, one lot of Dextrose 50%, and one lot of Hypertonic Saline, all of which are in the form of injectable fluids, to the user level. These injectable fluids are being recalled as a precautionary measure; because of departures from customary sterility procedures, sterility cannot be entirely assured.
Toro Recalls Zero Turn Riding Mowers Due to Fire Hazard
The idler pulley on Z Master mowers can rub against the fuel tank. This is the second recall of these lawn mowers.
Family Dollar Stores Recalls Optimus Tower Quartz Heaters Due to Overheating and Fire Hazards
The brand name Optimus and two temperature knobs appear on the portable electric heaters.
NEWMAR ( 13V169000 )
Dated: APR 30, 2013 Newmar Corporation is recalling certain model year 2013 Bay Star Sport, Ventana and Ventana LE and model year 2013-2014 Bay Star, Canyon Star and Dutch Star motorhomes. If the awning installation seq...
NEWMAR ( 13V170000 )
Dated: APR 30, 2013 Newmar Corporation is recalling certain model year 2012-2013 Canyon Star motorhomes manufactured August 4, 2011, through February 19, 2013, for failing to conform to the requirements of Federal Motor ...
XYMOGEN identifies allergen oversight by third-party manufacturer; issues recall of artriphen?
Nutraceutical company XYMOGEN in Orlando, Fla., is recalling artriphen, a product recommended for the support of healthy joint function, because it contains traces of the undeclared allergens soy and milk.
Surly Bikes Recalls Bicycle Forks Due to Fall Hazard
Surly Pugsley bike forks can bend above the disc brake mount.
Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU?s 626570609490, 827912089028, 626570617877, 626570615316, Velextra brand SKU?s 626570619475, 626570619475, 626570619475, 626570619475 , Amerect SKU?s 626570619031, 626570619598 capsules to the retail level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. Amerect is voluntarily recalled because it has the potential to contain undeclared tadalafil. Tadalafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the products unapproved new drugs.
Chang Kwung Issues A Voluntary Nationwide Recall of Lightning Rod Capsules Due to Undeclared Ingredient
2013 Chang Kwung announced today that it is conducting a voluntary nationwide recall of the company?s dietary supplements sold under the brand name Lightning Rod 500 mg per capsule packaged in 3-count, UPC 6 89076 20257 2 and 12-count bottles, UPC 6 89076 20297 8.
Chang Kwung is conducting a voluntary recall after being notified by the US FDA that analytical testing found the Lightning Rod Capsules to contain an analogue of Sildenafil.
KUMHO ( 13T004000 )
Dated: APR 30, 2013 Kumho Tire U.S.A., Inc. (Kumho) is recalling certain Kumho Solus KH25 passenger car tires, size 225/45R17, produced in the weeks of 3411 through 2512 (August 21, 2011 through June 23, 2012). The aff...
BMW ( 13V172000 )
Dated: MAY 03, 2013 BMW is recalling certain model year 2002-2003 325i, 325xi, 330i, 330xi sedans; 325Ci and 330Ci coupes and convertibles; 325iT and 325xiT Sports Wagons; and M3 coupes and convertibles to address a safe...
BUICK ( 13V173000 )
Dated: MAY 03, 2013 General Motors (GM) is recalling certain model year 2012 and 2013 Buick LaCrosse and Regal, and model year 2013 Chevrolet Malibu Eco vehicles equipped with eAssist. These vehicles may have a conditio...
CHEVROLET ( 13V173000 )
Dated: MAY 03, 2013 General Motors (GM) is recalling certain model year 2012 and 2013 Buick LaCrosse and Regal, and model year 2013 Chevrolet Malibu Eco vehicles equipped with eAssist. These vehicles may have a conditio...
WESTMOR ( 13V165000 )
Dated: APR 29, 2013 Westmor Industries, LLC. (Westmor) is recalling certain model year 2003-2013 trailers equipped with Fisher-branded H732 and H832 pressure relief valves, manufactured by Emerson Process Management Regu...
Cargill?s Animal Nutrition Business Conducts Voluntary Recall of Lamb Feed
Cargill?s animal nutrition business today announced a voluntary recall of Showmaster® S-Series Show Lamb Feed (BW) because it contained incorrect sodium molybdate levels. To date, there are 170, 50-pound bags of feed still out in the market.
FERRARA ( 13V167000 )
Dated: APR 25, 2013 HME is recalling certain model year 2012 Spectr Fire Apparatus, Spectr Chassis, and 2011-2012 Ferrara Intruder Ember Chassis vehicles manufactured January 26, 2011, through November 7, 2012. These ve...
HME ( 13V167000 )
Dated: APR 25, 2013 HME is recalling certain model year 2012 Spectr Fire Apparatus, Spectr Chassis, and 2011-2012 Ferrara Intruder Ember Chassis vehicles manufactured January 26, 2011, through November 7, 2012. These ve...
JAYCO ( 13V168000 )
Dated: APR 30, 2013 Jayco is recalling certain model year 2013-14 Eagle Premiere, Jay Feather Ultra Lite, Jay Flight, Jay Flight Swift, Octane, and White Hawk; model year 2013 Eagle, Eagle HT, Jay Flight Bungalow, Jay Fl...
MERCEDES ( 13V166000 )
Dated: APR 26, 2013 Mercedes-Benz USA, LLC (Mercedes) is recalling certain model year 2013 GL350 BlueTEC, GL450 4MATIC, GL550 4MATIC, and GL63 AMG vehicles manufactured May 15, 2012 through October 4, 2012. The second ro...
Nestle USA Announces Voluntary Recall of Select Varieties/Production Codes of California Pizza Kitchen and DiGiorno Frozen Pizzas
Nestlé USA?s Pizza Division today announced the voluntary recall of select production codes of four different frozen pizzas sold in the U.S. These include:
? California Pizza Kitchen (CPK) Crispy Thin Crust White®, UPC 71921 98745; production codes are 3062525951, 3062525952 and 3063525951.
Medtronic Announces FDA Classification Of Deep Brain Stimulation Lead Cap Communication
In keeping with its commitment to keep physicians informed about product performance and safety, Medtronic, Inc. (NYSE: MDT) issued an Urgent Medical Device Correction notification in February 2013 to provide physicians with information concerning the potential for deep brain stimulation (DBS) lead damage associated with the use of the lead cap provided in Medtronic DBS lead kits and dystonia therapy kits.
ITASCA ( 13V162000 )
Dated: APR 26, 2013 Winnebago Industries, Inc. (Winnebago) is recalling certain model year 2013-2014 Winnebago Access, Aspect, Sightseer, Vista, Adventurer, Forza and Itasca Impulse, Cambria, Sunova, Sunstar, Suncruiser ...
LIBERO ( 13V156000 )
Dated: APR 19, 2013 Triple E Recreational Vehicles (Triple E) is recalling certain model year 2012-2013 Libero L24CB, Serenity S24CB, Regency GT (GT24MB, GT27S, GT28D, GT29T), and Unity (U24CB, U24IB, U24TB, U24MB). The...
REGENCY GT ( 13V156000 )
Dated: APR 19, 2013 Triple E Recreational Vehicles (Triple E) is recalling certain model year 2012-2013 Libero L24CB, Serenity S24CB, Regency GT (GT24MB, GT27S, GT28D, GT29T), and Unity (U24CB, U24IB, U24TB, U24MB). The...
SERENITY ( 13V156000 )
Dated: APR 19, 2013 Triple E Recreational Vehicles (Triple E) is recalling certain model year 2012-2013 Libero L24CB, Serenity S24CB, Regency GT (GT24MB, GT27S, GT28D, GT29T), and Unity (U24CB, U24IB, U24TB, U24MB). The...
THOR ( 13V164000 )
Dated: APR 25, 2013 Thor Motor Coach is recalling certain model year 2013-2014 Challenger, Four Winds 5000, Hurricane, Chateau, Chateau Sport, and Windsport; model year 2013 Palazzo and Four Winds Siesta and model year 2...
TOYOTA ( 13V163000 )
Dated: APR 25, 2013 Toyota Motor Corporation (Toyota) is recalling certain model year 2007-2013 FJ Cruiser vehicles manufactured January 25, 2006 through February 23, 2013 and equipped with a Toyota Auxiliary Driving Lam...
UNITY ( 13V156000 )
Dated: APR 19, 2013 Triple E Recreational Vehicles (Triple E) is recalling certain model year 2012-2013 Libero L24CB, Serenity S24CB, Regency GT (GT24MB, GT27S, GT28D, GT29T), and Unity (U24CB, U24IB, U24TB, U24MB). The...
WINNEBAGO ( 13V162000 )
Dated: APR 26, 2013 Winnebago Industries, Inc. (Winnebago) is recalling certain model year 2013-2014 Winnebago Access, Aspect, Sightseer, Vista, Adventurer, Forza and Itasca Impulse, Cambria, Sunova, Sunstar, Suncruiser ...
American Lifestyle Issues a Worldwide Voluntary Recall of Vicerex Capsules and Black Ant Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
May 1, 2013 - American Lifestyle is announcing that it is conducting a voluntary recall of all lots of Vicerex UPC 893490820087 and Black Ant UPC 4026666142546. Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil.
ITASCA ( 13V161000 )
Dated: APR 22, 2013 Winnebago Industries is recalling certain model year 2012-2014 Minnie Winnie, Chalet, Aspect, Sightseer, Adventurer, and Journey motorhomes; and model year 2012-2014 Itasca Spirit, Cambria, Sunova, Su...
TEREX ( 13V160000 )
Dated: APR 24, 2013 Terex South Dakota, Inc. (Terex) is recalling certain model year 1998-2005 OM Aerial Devices used on utility trucks. The leveling arm at the elbow can develop fatigue cracks.
WINNEBAGO ( 13V161000 )
Dated: APR 22, 2013 Winnebago Industries is recalling certain model year 2012-2014 Minnie Winnie, Chalet, Aspect, Sightseer, Adventurer, and Journey motorhomes; and model year 2012-2014 Itasca Spirit, Cambria, Sunova, Su...
LEM Products Distribution Recalls 5-Tray Food Dehydrators Due to Fire Hazard
The fan in the 5-tray food dehydrator can fail and cause the product to overheat and catch fire.
Louisville Slugger OneX Fastpitch Softball Bats Recalled by Hillerich & Bradsby Due to Injury Hazard from Breakage
The bat's barrel can separate from the handle during use. The company has received 170 reports of bat separations.
KEYSTONE ( 13V155000 )
Dated: APR 22, 2013 Keystone RV Company (Keystone) is recalling certain model year 2013-2014 recreational trailers equipped with Dometic 9100 Power Awnings or Weather Pro awnings, awning serial numbers 306xxxx through 31...
Carson?s Deli & Bakery Issues Allergy Alert For Undeclared Allergens In Assorted Cookie Pack And Fudge Brownie Cookie
CARSON?S DELI & BAKERY of Lockport, NY is recalling 200 packages of ASSORTED COOKIE PACK, UPC 7 53182 15240 0, and FUDGE BROWNIE COOKIES, UPC 7 53182 15240 0 because they contain undeclared allergens. Carson?s Assorted Cookie Pack contains undeclared walnuts, wheat flour, milk and peanut butter.
Prime Food USA Issues an Alert on Listeria in Latis Brand Herring Fillet "Antalja" in Oil and Latis Brand Herring Fillet in Oil with Spices
Prime Food USA, 50st & 1st Ave Building # 57, Brooklyn NY 11232, is recalling Latis Brand Herring Fillet ?Antalja? in Oil and Latis Brand Herring Fillet in Oil with Spices due to contamination with listeria monocytogenes.
Listeria can cause serious complications for pregnant women, such as stillbirth.
Krinos Foods, LLC. Voluntarily Recalls Tahini Jars Because of Possible Health Risk
Krinos Foods, LLC. of Long Island City, New York is voluntarily recalling its TAHINI sesame paste, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Voluntary Nationwide Recall of 15 Lots of Piperacillin and Tazobactam for Injection, USP 40.5 Grams Due to Possibility of Precipitation / Crystallization in IV Bag or IV Line Upon Reconstitution
WESTON, FL, April 26, 2013 /CNW/ - Apotex Corp. announced today that it is conducting, on behalf of the manufacturer Hospira, Inc., a voluntary nationwide recall of 15 lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams, NDC number 60505-0773-00 to the hospital / healthcare provider /user level. The impacted lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams may show precipitation / crystallization in IV bag or IV line after reconstitution.
Smart & Final issues Recall - Allergy Alert Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini
Smart & Final of Los Angeles, Calif. is recalling 2.5 lb. La Romanella Tri-Color Cheese Tortellini because it may contain undeclared wheat, eggs and milk. People who have an allergy or severe sensitivity to wheat, eggs and /or milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Maple View Farm Recalls Three Flavors of Ice Cream Because of Undeclared Allergens
Maple View Farm is voluntarily recalling pint containers of Cookies & Cream, Carolina Crunch and Cookie Dough ice cream because the products contain allergens that were not declared on package labels. Some or all of the products contain wheat,soy, almonds and peanuts, which can cause serious allergic reactions in people who have an allergy or sensitivity to these ingredients.
Orville Redenbacher?s® Classic Kettle Korn Ready-to-eat Popcorn Recalled Due to Undeclared Milk Allergen
Today, ConAgra Foods, Inc., (NYSE: CAG) in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling packages of its Orville Redenbacher?s Classic Kettle Korn flavor ready-to-eat popcorn that may contain an undeclared allergen, milk. Certain bags of the Kettle Korn flavored ready-to-eat popcorn may have inadvertently been filled with white cheddar flavored popcorn, which contains an allergen, milk.
HONDA ( 13V157000 )
Dated: APR 23, 2013 Honda is recalling certain model year 2012-2013 Honda Fit Sport vehicles manufactured May 23, 2011, through March 22, 2013. The electronic stability control system of the affected vehicles may allow ...
NISSAN ( 13V158000 )
Dated: APR 23, 2013 Nissan North America is recalling certain model year 2013 Altima vehicles manufactured March 21, 2012, through March 26, 2013. The spare tires may have been significantly over- or under-inflated.
Saratoga Therapeutics, LLC Issues Allergy Alert on Undeclared Milk Components in Eba Multivitamin Supplement
April 23, 2013 - Saratoga Therapeutics, LLC of North Wales, PA is recalling 900 bottles of ebA Multivitamin Supplement because they may contain undeclared milk components ?milk protein(s) and lactose. The following lot numbers may be affected:
# 0912164 expiration date 12/12
# 1110354 expiration date 10/14
People with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction and people who have lactose intolerance run the risk of gastrointestinal symptoms if they consume ebA Multivitamin Supplement.
Hospira Issues a Voluntary Nationwide Recall of One Lot Of 0.9% Sodium Chloride Injection, Usp, 100 Ml, Flexible Containers Due to Particulate ? Revised to Update Stericycle Phone Number
Hospira, Inc. (NYSE: HSP), announced today that last August it initiated a voluntary nationwide user-level recall of one lot of 0.9% Sodium Chloride Injection, USP, 100 mL, Flexible Container, NDC 0409-7984-23. This action was due to one confirmed customer report where four separate particulate issues were identified in four individual flexible containers.
BMW ( 13V154000 )
Dated: APR 19, 2013 BMW is recalling certain model year 2013 R1200 GS motorcycles manufactured January 9, 2013, through February 8, 2013. Due to an insufficient torque of a locking bolt, the front fork tube may loosen.
SHASTA REVERE ( 13V151000 )
Dated: APR 19, 2013 Forest River is recalling certain model year 2013 Shasta Revere model SHT27DB, SHT30BH, SHT27BH, SHT26TB, and SHT27KS trailers manufactured September 4, 2012, through April 10, 2013. These vehicles w...
SUBARU ( 13V159000 )
Dated: APR 24, 2013 Subaru is recalling certain model year 2014 Forester vehicles manufactured from January 2013 through March 2013. The backing for the carpeted floor mats was not manufactured to specification. As a re...
Potential for Delivery System Catheter Separation Prompts Cook Medical to Initiate Voluntary Global Recall of Zilver® PTX® Drug Eluting Stent
Based on its investigation into a small number of complaints that the delivery system of the device had separated at the tip of the inner catheter, Cook Medical has initiated a nationwide/global voluntary recall of its Zilver® PTX® Drug Eluting Peripheral Stent. Cook received 13 complaints of delivery system tip separation with an occurrence rate of 0.043 percent.
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