Archive
297 recalls were announced in February 2013.
Of the 297 recalls this month scored against our rubric, 3% are Critical, 18% are Severe.
Which agencies issued them
Spartan Motors is recalling 2012-2013 Metro Star and Gladiator fire trucks because a short circuit in the air bag control module could cause unintended deployment.
Progressive Dynamics is recalling specific RV power converters because internal components may short circuit, posing a fire risk.
Keystone is recalling 2013 Montana and Fuzion Fifth Wheel vehicles because a power converter component may short circuit and cause a fire.
Supreme is recalling 2009-2010 Startrans MFSAB school buses with Ricon wheelchair lifts due to a potential fire hazard from an armored cable.
Balsam Hill is recalling about 700 pre-lit artificial Christmas trees because the remote control receiver box can overheat and melt, posing burn and shock risks.
Supreme Corporation is recalling 2006-2012 Startrans buses with Ricon wheelchair lifts because an armored cable may cause a short circuit and fire.
SlumberWorld is recalling approximately 810 mattresses sold in Hawaii from 2011 to 2012 because they fail to meet the mandatory federal open flame standard, posing a fire hazard.
Mylan Institutional, Inc. is recalling specific lots of Hydrocodone Bitartrate and Acetaminophen Tablets because the tablets are oversized, resulting in superpotent assays of both active ingredients.
P & J Trading Co is recalling Slimdia Revolution capsules because they contain sibutramine, a drug removed from the U.S. market for safety reasons.
Hill-Rom is recalling Liko Overhead Rail Systems because hardware corrosion in high-humidity areas caused two rail failures.
Meritor is recalling axle assemblies with specific air brake chambers that may leak pressure, causing brake dragging and potential fire.
Tumalo Farms LLC is recalling specific batches of Chevita soft cheese due to improper pasteurization. The product was distributed in Washington and Oregon.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 19 NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves because the taper connection may fracture under normal gait loads.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves due to a potential fracture risk at the taper junction during normal gait activities.
Tumalo Farms LLC is recalling 222 six-ounce pucks of Jewell soft brie-style cheese because it was improperly pasteurized. The product was distributed in Washington and Oregon.
Bimbo Bakeries USA is recalling Sara Lee Deluxe Bagels in four varieties because metal fragments were found in two packages.
Codman & Shurtleff is recalling 56 NeuroPath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 266 units of NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling Neuropath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility. The recall covers 10 units distributed worldwide.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Greiner Bio-One is recalling VACUETTE Safety Blood Collection Sets because a crack in the luer connector may cause small droplets of blood to leak during use.
Codman & Shurtleff is recalling 268 units of Neuropath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Medrad Inc is recalling Hand Controller Sheaths because a missing seal may compromise sterility. The product is used in cardiac catheterization procedures.
Bimbo Bakeries USA is recalling Weight Watchers 6 Original Bagels because metal fragments were found in two packages.
Bimbo Bakeries USA is recalling Publix Premium Bagels because metal fragments were found in two packages. Consumers should stop eating the product.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
CareFusion is recalling 5,050 units of SmartSite Gravity Blood Sets because the drip chamber and tubing may separate, potentially delaying treatment.
Elekta is recalling 13 Monaco RTP Systems because the beam is displayed at the gantry angle, but the dose is calculated at the rotation_start angle.
ConMed is recalling Electrolase Hyfrecator electrodes because some sterile pouch seals were compromised, potentially affecting sterility.
Codman & Shurtleff is recalling 25 NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 141 units of NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves because the taper connection may fracture under normal physiologic loads.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 1,548 NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
International Technidyne Corp. is recalling specific lots of Pro Time 3 Cuvettes because they may produce lower than expected Prothrombin Time/INR results.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves because the taper connection may fracture under normal gait loads.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Liberty Mountain is recalling Singing Rock Easy Go XP Lock Via Ferrata Lanyards because the elastic webbing can break, posing a risk of serious injury or death.
Jerdon Style is recalling about 6,000 one-cup coffeemakers because they can overheat, posing fire and burn hazards. No injuries have been reported.
Integra LifeSciences is recalling 96 MAYFIELD Composite Series Base Units because they may break during use, posing a risk to patients during surgical procedures.
Animas Corporation is recalling insulin infusion pumps that will stop operating on January 1, 2016, due to an internal calendar date limit.
Codman & Shurtleff is recalling Neuropath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Varian Medical Systems is recalling 1,168 units of the Eclipse Treatment Planning System because the Pencil Beam Convolution 11.0 algorithm incorrectly calculates dose for dynamic plans with different energy fields.
Maquet is recalling ELS 15 FR Cannulas used for infant ECMO because they may contain an occluded arterial lumen.
Vascular Solutions, Inc. is recalling SuperCross Microcatheters due to potential surface contamination on aged units discovered during in-house testing.
Codman & Shurtleff is recalling 867 NeuroPath guiding catheters because packaging defects may compromise sterility. The devices were distributed worldwide.
Philips is recalling 3,785 HeartStart XL+ defibrillators because they may become locked out of clinical use.
Nestle USA is recalling Lean Cuisine Mushroom Mezzaluna Ravioli because consumers reported finding small fragments of glass inside the product.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility. The recall covers 34 units distributed worldwide.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Merit Medical Systems is recalling 387 Resolve Biliary Locking Drainage Catheters because a consumer reported the device broke into several pieces during use.
Bimbo Bakeries is recalling specific varieties of Thomas' Bagels because metal fragments were found in two packages. Consumers should check their packages and stop eating them.
Procter & Gamble is recalling Crest Pro-Health Oral Rinse because it was mixed with another type of mouthwash.
ConMed is recalling specific lots of Electrolase Hyfrecator electrodes because some sterile pouch seals were compromised, potentially affecting sterility.
Ansell Healthcare Products LLC is voluntarily recalling LifeStyles ZERO 10 latex condoms due to complaints about difficulty unrolling and breakage.
Stryker is recalling AC Power Adaptors for the Restep DVT System because wires may come loose, preventing the unit from operating.
Healthtronics, Inc. is recalling 50 units of Endocare 3.8mm RenalCryo Cryoprobes because the outer box labels display incorrect expiration dates.
Dynacraft is recalling Hello Kitty City Motor Scooters because they can accelerate suddenly, causing riders to lose control and fall.
US Specs is recalling four vehicles to correct incorrect font size labels on passenger side mirrors, which may hinder drivers' ability to judge object proximity.
Robert Bosch LLC is recalling specific Hydro-Max brake master cylinders because the fluid level indicator may fail to warn drivers of low brake fluid, potentially increasing crash risk.
One World Technologies is recalling Ryobi Lithium 18 V 4Ah battery packs because they can overheat and burst while charging, posing fire and burn risks.
Dynacraft is recalling about 5,500 Monster High City Motor Scooters sold at Walmart because they can accelerate suddenly, causing riders to lose control and fall.
US Specs is recalling one 2002 Porsche 911 Carrera because passenger seatbelts lack the required Automatic Locking Retractor function, posing a risk to child restraints.
Quadratec is recalling aftermarket driver-side floor liners for 2007-2013 Jeep Wranglers because they may tear and shift forward, potentially impeding the accelerator pedal.
Northwood is recalling specific 2013 model year trailers because incorrect information on federal identification and weight labels could lead to improper loading and axle failure.
Pierce Manufacturing is recalling 2007-2010 Velocity and Impel fire trucks because inner door handle springs may allow doors to open inadvertently while in motion.
Subaru is recalling certain 2010-2013 vehicles equipped with Audiovox remote engine starter accessories because the fobs may malfunction and start the engine without user input.
Daimler Buses North America is recalling 2011-2012 Orion VII buses because leaking brake chambers may cause the parking brake to drag, potentially leading to overheated components and fire.
Fontaine Heavy-Haul is recalling 78 model year 2013 Renegade LX40 and LXT40 lowbed trailers because a connecting plate may crack and fail, increasing crash risk.
Porsche is recalling 2012-2013 911 Carrera and Carrera 4 vehicles because the exhaust tail pipe may fracture and separate, posing a hazard to other vehicles.
OWT Industries is recalling about 131,500 Expert Gardener electric blower vacuums sold at Walmart because objects can break through the housing, posing a laceration hazard.
Homelite is recalling electric blower vacuums sold at Home Depot because objects can break through the housing, posing a laceration hazard.
H-E-B is recalling General Joe's chicken deli products in Texas because they may be contaminated with salmonella. Consumers should not eat the recalled items.
Hoop Nuts LLC is recalling dry roasted pistachios due to Salmonella contamination. The recall affects 20 cases distributed in California.
Hoop Nuts LLC is recalling raw pistachios due to Salmonella contamination. The recall affects 20 cases of 30-pound boxes distributed in California.
Diversified Foods & Seasonings is recalling Cheesy Broccoli Soup because a consumer found shrimp in the product. The recall covers 189 cases distributed in Tennessee and Mississippi.
Pamela's Products is recalling 1,709 cases of Chocolate Chunk Cookie Mix due to potential glass or plastic fragments.
H-E-B is recalling four varieties of deli sesame chicken products sold in Texas due to potential salmonella contamination.
He Butt Grocery Company is recalling HEB Deli Sweet and Sour Chicken products in Texas due to potential Salmonella contamination.
Lee Pharmaceuticals is recalling 12-Hour Sinus Nasal Spray products due to microbial contamination identified during testing.
Tropical Nut & Fruit Co. is recalling 1,380 lbs of Chia ReCharged Stix Mix due to undeclared peanuts. The product was distributed in Florida and North Carolina.
GE Healthcare is recalling 276 Giraffe and Panda T-Piece Resuscitation Systems because oxygen and air inlet fittings were reversed during assembly.
H-E-B is recalling specific Lemon Grass Chicken deli products in Texas due to potential Salmonella contamination.
Aesculap, Inc. is recalling 11 units of the Miethke Shunt System because the deflector may not move freely on the ventricular catheter.
NAImco Inc dba Richmar Inc is recalling foam electrodes where the socket terminal may pull away from the lead wire. The defect poses a risk of electrical shock or injury.
Lockheed Martin Gyrocam Systems are being recalled because they contain Class IIIb lasers that failed FDA performance standards and were sold without a required variance.
Remel Inc is recalling 50 units of the Xpect Clostridium difficile Toxin A/B test kit due to a potential for false negative results.
Mindray is recalling 51 DPM Central Monitoring Systems because a software anomaly may display a step pattern instead of a flat line during asystole.
Terumo is recalling 622 CDI 101 Hematocrit/Oxygen Saturation Monitoring Systems because software errors cause inaccurate readings of blood and oxygen levels.
NAImco Inc dba Richmar Inc is recalling cloth electrodes where the socket terminal may pull away from the lead wire.
Suadel Food Products is recalling Estrella Pastelillos de Pizza because the common name 'milk' is not declared in the ingredients or 'Contains' statement.
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