Archive
399 recalls were announced in June 2014.
Of the 399 recalls this month scored against our rubric, 7% are Critical, 23% are Severe.
Which agencies issued them
The Manischewitz Company is recalling Tam Tams Snack Crackers Original due to rancidity. The recall covers 29,413 units distributed nationwide.
Gen-Probe Inc is recalling APTIMA Urine Collection Kits because inner pouches are mislabeled as swab collection kits.
The Manischewitz Company is recalling Tam Tams Snack Crackers Garlic due to rancidity. The recall covers 29,413 units distributed nationwide.
Convatec Inc. is recalling the Flexi-Seal Fecal Management System because it lacks FDA 510(k) clearance and its Auto-Valve feature is not performing consistently.
Suzuki is recalling 2004-2006 Verona vehicles because heat in the daytime running light module could melt and cause a vehicle fire.
Piaggio is recalling 2013 Vespa 946 scooters because a fuel line may leak, potentially causing stalling or fire.
Hyundai is recalling 16,900 2015 Sonata vehicles because front brake calipers may fracture, reducing braking effectiveness and increasing crash risk.
Stile Products is recalling specific Tern folding bicycles because the frame can crack at the hinge, posing a fall hazard. No U.S. injuries have been reported.
Trane recalls about 100,600 air conditioning units because defective ground screws may not provide sufficient grounding, posing a shock hazard.
Gillig is recalling 2007-2014 Low Floor transit buses because an oil sampling hose may leak near hot exhaust components, increasing the risk of fire.
General Motors is recalling specific Buick, Cadillac, and Chevrolet models because the ignition switch may move out of the run position, potentially preventing airbag deployment and causing loss of power steering and braking.
Sunright is recalling Rodia RDH 500 motorcycle helmets manufactured in late 2009 because they may not adequately protect the head in a crash.
Palfleet is recalling 2009-2013 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific PTO assemblies because oil leaks may cause a fire.
Spartan is recalling 2013-2014 Gladiator emergency vehicles because a fuel fitting may wear and leak, increasing fire risk.
Wei-Chuan USA is recalling Pork Mini Buns containing crab meat because the label failed to declare fish, shellfish, and egg allergens.
General Motors is recalling 2010-2014 Chevrolet Camaros because the ignition key may be accidentally knocked out of the run position by the driver's knee, potentially disabling airbags and power steering.
Honda is recalling specific 2003-2006 vehicles sold or registered in California due to a Takata air bag inflator defect that could rupture during deployment.
Volvo is recalling 2011-2015 VNL and 2014-2015 VNM trucks because the active braking component of the enhanced cruise control can become disabled, increasing crash risk.
Bellisio Foods is recalling Thai Kitchen Chicken Pad Thai frozen entrées because the packaging fails to list soy protein isolate, a known allergen.
General Motors is recalling 2013-2014 Cadillac ATS and 2014 CTS vehicles because the transmission shift cable may detach, causing unintended movement or rollaway.
Altec is recalling 258 aerial trucks because front torsion bar welds could fail, potentially causing vehicle instability and injury to the operator.
General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD trucks because a power steering hose clamp may disconnect, potentially causing loss of steering and brake assist.
General Motors is recalling 2014 Chevrolet Corvettes with optional sport seats because they do not meet injury protection specifications for unbelted young children.
General Motors is recalling 2011 Cadillac CTS vehicles because drive shaft vibrations may trigger roof rail air bags, increasing crash risk.
James A. Kiley is recalling 2010-2013 Terex utility vehicles because oil may leak from the PTO pressure switch onto the exhaust, increasing fire risk.
Dearborn Sausage Company is recalling approximately 3,660 pounds of slab bacon because the product contains hydrolyzed soy protein, a known allergen, that is not declared on the label.
Reebok is recalling specific goalie throat collars because skate blades could penetrate the material, posing a risk of throat laceration. No injuries have been reported.
Linear LLC is recalling about 175,000 Personal Emergency Reporting System (PERS) transmitters because the batteries may fail to emit a low battery warning, leaving users unaware the device is not functioning.
Pure Edge Nutrition is recalling Bella Vi BTrim Ultimate Boost capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Meizitang Strong Version Botanical Slimming capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine.
MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.
MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.
Vitality Research Labs is recalling vitaliKOR capsules because FDA sampling found undeclared vardenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
MyNicNaxs, Inc. is recalling Jianfeijindan Activity Girl Capsules because they contain an undeclared sibutramine analog and were marketed without FDA approval.
Pure Edge Nutrition is recalling Bella Vi AMP'D UP weight loss capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicKnaxs is recalling weight reduction pills marketed without FDA approval because they contain undeclared phenolphthalein.
MyNicNaxs, Inc. is recalling REDUCE WEIGHT FRUTA PLANTA Capsules because they contain undeclared phenolphthalein and were marketed without FDA approval.
Pharmakon Pharmaceuticals is recalling specific lots of Midazolam syringes because they contain twice the stated amount of the drug.
MyNicNaxs, Inc. is recalling Super Fat Burning Bomb Capsules because they contain undeclared active pharmaceutical ingredients, phenolphthalein and N-desmethylsibutramine.
Greenstone LLC is recalling 16,018 bottles of Venlafaxine HCl Extended-Release Capsules because a foreign capsule was found in a bottle from the same packaging campaign.
Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling SlimEasy Herbs Capsules because they contain undeclared sibutramine and N-desmethylsibutramine and were marketed without an approved NDA/ANDA.
Pure Edge Nutrition is recalling Bella Vi eXtreme ACCELERATOR capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi INSANE Bee Pollen capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.
Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D dietary supplements because they contain undeclared sibutramine and phenolphthalein.
T.H. Seafood Inc. is recalling raw, frozen black cod because the packaging lacks instructions to keep the product frozen or refrigerated after thawing.
Cordis Corporation is recalling 80 units of EMPIRA RX PTCA Dilatation Catheters because they may exhibit radial versus axial tears if they burst during inflation.
T.H. Seafood Inc. is recalling raw, frozen, vacuum-packaged salmon because the labeling failed to instruct consumers to keep the product frozen or thawed under refrigeration to control Clostridium botulinum.
Dual-Tech is recalling 2009-2014 modified Ford F-550 trucks because oil leaks from a PTO switch may ignite the exhaust thermal blanket.
Siemens Healthcare Diagnostics is recalling four Vista Air Compressors because miswiring could cause a fire or electrical shock if powered up.
Cubist Pharmaceuticals is recalling 51,500 vials of CUBICIN (daptomycin) because a customer reported a glass shard in one vial.
T.H. Seafood Inc. is recalling approximately 2,000 lbs of raw, frozen rockfish because packaging labels failed to instruct consumers to keep thawed fish under refrigeration to control Clostridium botulinum.
General Motors is recalling specific 2014 Chevrolet Silverado and GMC Sierra trucks because optional floor mats may not be secured, potentially interfering with the accelerator pedal.
MCI is recalling specific 1993-1995 and 2006-2008 motor coaches because the driveshaft may detach, potentially causing loss of steering control and increasing crash risk.
Hot Pandeyuca & Company Inc. is recalling Cheese Bread Pan de Queso Grande because the label failed to declare allergens in a butter flavor.
Philips is recalling IntellVue Info Center monitors because a software defect causes reboot loops that interrupt patient monitoring.
Alere San Diego, Inc. is recalling 373 kits of the Alere Triage D-Dimer Test (Lot W53884B) because they may generate error codes or incorrect results.
Hot Pandeyuca & Company Inc is recalling Soft Bread Pan Alinado because the label failed to declare allergens in a butter flavor.
Brooks Furniture is recalling glider rockers sold to Kaplan Early Learning because spindles can separate, posing a fall hazard. No injuries have been reported.
Nokia is recalling travel charger kits for the Lumia 2520 tablet because loose plastic covers can expose internal components, posing an electrocution risk.
Fischer & Wieser Specialty Foods is recalling Harry & David Wild 'N Spicy Dos Quesos Dip due to undeclared wheat. The recall affects 2,712 glass jars distributed in Ohio and Oregon.
Stryker is recalling 285 sterile 3.0mm Round Fluted Bur Aggressive devices due to missing or partial notches. The defect may affect the device's compatibility with Elite Attachments.
Fischer & Wieser Specialty Foods is recalling 636 jars of Harry & David Wild 'N Spicy Jalapeno Tomato Cheese Dip due to undeclared wheat.
Leica Microsystems is recalling 103 MSF-1 ceiling mounts because a broken drive screw caused the lift arm to fall approximately 60 cm.
Neo Metrics, Inc. is recalling NovaGold High Performance Guidewires because the tip may uncoil or detach more frequently than anticipated. No illnesses or injuries have been reported.
Teleflex Medical is recalling 450 Taut Operative Cholangiogram Catheters because the metal support tube is missing. The recall covers units distributed in the US and Belgium.
CooperSurgical is recalling 1,180 units of the Tampa Catheter because unsealed pouches may compromise the device's sterility.
Maquet is recalling PowerLED 700 surgical lights because plastic tabs may break, causing the ambient light module to partially detach.
Leica Microsystems is recalling 103 ceiling mounts for M500 N microscopes because a broken drive screw caused the lift arm to fall approximately 60 cm.
BioDerm, Inc. is voluntarily recalling skin-prep wipes used with external male catheters due to potential bacterial contamination.
United Bakery is recalling Parmesan Bread Sticks because egg is an ingredient in the cheese but is not declared on the label.
T.H. Seafood Inc. is recalling raw, frozen halibut because the packaging lacks instructions to keep thawed fish under refrigeration, posing a Clostridium botulinum risk.
BioDerm, Inc. is voluntarily recalling specific skin wipes used in male incontinence devices due to potential bacterial contamination from a contract manufacturer.
Ivoclar Vivadent is recalling 241 Bluephase style light probes because a stock check revealed broken glass fibers between the connector and the fiber bundle.
Legacy Pharmaceutical Packaging is recalling Pantoprazole Sodium tablets because some cartons may contain Lorazepam tablets instead.
Hot Pandeyuca & Company Inc is recalling Small Cheese Bread Quesipan because the label failed to declare allergens in a butter flavor.
BioDerm, Inc. is voluntarily recalling skin-prep wipes used with external male catheters due to potential bacterial contamination.
Diamond Crystal Brands is recalling Poco Pac Salad Dressing packets because they contain egg, which is not listed on the label.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems due to a potential for biased results when using Multiple Window codes.
Philips is recalling IntelliVue MX40 monitors because alarms may not resume after being paused, potentially delaying clinical response.
Stryker is recalling 176 sterile 1.3mm Wire Pass Drills because some units may have missing or partial notches.
Stryker is recalling 802 sterile neuro drill accessories due to missing or partial notches that may affect compatibility with Elite attachments.
Stryker is recalling 62 units of 4.5mm Round Fluted Bur Aggressive Sterile devices due to missing or partial notches.
Teleflex Medical is recalling 1,000 RUSCH Easy Cath Coude Kits because they were packaged with straight catheters instead of the required curved ones.
Stryker is recalling four sterile Zyphr Elite Round Fluted Bur units due to missing or partial notches that may affect compatibility with Elite attachments.
Stryker is recalling 2.0mm Tapered Round Elite Burs because some units have missing or partial notches. The devices are used for cutting bone during surgery.
McKesson Medical Imaging is recalling Horizon Medical Imaging software after a complaint that an unreported study could not be opened from the archive.
Ortho-Clinical Diagnostics is recalling enGen Laboratory Automation Systems with specific TCAutomation software versions due to a potential delay in reporting patient sample test results.
Stryker is recalling 301 sterile 6.0mm Round Fluted Bur Aggressive devices because some units have missing or partial notches.
Stryker is recalling 65 units of 6.0mm Egg Bur sterile surgical instruments because some units have missing or partial notches.
Cenorin LLC is voluntarily recalling 25 HLD Systems Model 610 Washer/High Level Disinfector units because they may not inject the proper amount of cleaning fluid, potentially failing to reduce debris.
Stryker is recalling 41 sterile neuro drill accessories due to missing or partial notches that may affect compatibility with Elite attachments.
Stryker is recalling 99 sterile 5.5mm Round Fluted Bur Soft Touch devices because some units may have missing or partial notches.
Stryker is recalling 59 sterile 6.0mm Acorn Burs because some units have missing or partial notches, which may affect their use with Elite Attachments.
Mandelin Inc is recalling marzipan products containing undeclared Yellow #5 and #6 dyes. The affected items were distributed in California, Kentucky, and Colorado.
Smiths Medical ASD, Inc. is recalling one lot of Portex Low Dead Space Connectors with Sideport because 3.0mm devices were packaged and labeled as 3.5mm.
La Terra Fina Inc. is recalling specific lots of Spinach & Kale Dip and Spread because one lot's ingredient statement incorrectly lists ingredients for spinach dip.
Dr. Reddy's is recalling specific lots of Metoprolol Succinate Extended Release Tablets because they failed dissolution testing at 18 months.
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