Archive
533 recalls were announced in June 2013.
Of the 533 recalls this month scored against our rubric, 5% are Critical, 33% are Severe.
Which agencies issued them
Altec is recalling 2008-2009 Lift-All LSS aerial devices because cracks in the turntable may cause failure, increasing the risk of personal injury.
Prevost is recalling 27 model year 2013 and 2014 X3-45 coaches because tail lamps are too bright, which may confuse following drivers and increase crash risk.
BMW is recalling 2013 F700 GS and F800 GS motorcycles because a damaged side-stand switch may allow the engine to run while the stand is down, increasing crash risk.
LDV, Inc. is recalling 2012-2013 mobile specialty vehicles because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing injury or crash risk.
Starcraft is recalling 36 model year 2014 Launch Ultra Lite travel trailers because incorrect cargo capacity labels may lead to tire overloading and failure.
La Boit is recalling 2013 Mobile Services vehicles because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing crash risk.
General Motors is recalling specific 2012 Chevrolet Volt vehicles because a brake pressure modulator valve issue may cause front brakes to lock up during safety system events.
Eldorado National is recalling 2011-2013 Amerivan Toyota Sienna vans because the fuel filler neck may contact the shock absorber, risking a fire.
Stile Products is recalling approximately 175 Tern folding bicycles because the frame hinge can crack, posing a fall hazard. Consumers should stop riding and contact the company for a free frame replacement.
Fred & Friends is recalling Buff Baby baby rattles because the end caps can separate, creating a choking hazard for small children.
Swan Creek Candle Co. is recalling about 715,000 loose votive candles because they can burn with high or erratic flames, posing a fire and burn risk.
Logan Coach is recalling 2013 Razor 3-Horse Gooseneck trailers because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing injury risk.
Altec is recalling 2002-2010 AH75, AH85, and AH100 aerial devices because cracks in the pedestal may cause the device to fail, increasing the risk of personal injury.
Sequel Naturals Ltd is recalling Vega Sport Natural Plant-Based Protein Bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.
Sequel Naturals Ltd is recalling Vega One Double Chocolate nutrition bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.
Sequel Naturals Ltd is recalling Vega Sport Chocolate Coconut protein bars because milk ingredients were inadvertently added to the chocolate coating. One allergic reaction has been reported.
Sequel Naturals Ltd is recalling Vega One chocolate almond nutrition bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.
Sequel Naturals Ltd is recalling Vega One chocolate cherry nutrition bars because milk ingredients were inadvertently added to the chocolate coating.
Hospira is recalling 676,872 containers of 0.9% Sodium Chloride Injection due to a potential leak at the administrative port that compromises sterility.
Respironics is recalling V60 ventilators due to a software issue on the Power Management Board Assembly that could cause loss of ventilator support without an audible alarm.
Volvo is recalling 23,056 heavy-duty trucks from 2007-2014 because a missing redundant switch may prevent the clutch from disengaging, increasing stopping distance.
Sagent Pharmaceuticals is recalling Vecuronium Bromide for Injection because it was not manufactured under current good manufacturing practices, resulting in failed impurity specifications.
Pharmacia & Upjohn LLC is recalling specific lots of Cleocin Phosphate injection vials due to the presence of very small reflective flakes consistent with glass delamination.
Conagra is recalling Lightlife Farmer's Market Veggie Burgers because packaging may contain milk-containing products, and the milk allergen is not declared on the label.
Biomet is recalling 17 units of the Superior Approach Resection Guide Assembly because a manufacturing defect may prevent the guide from securing properly to bone during surgery.
Teva Pharmaceuticals is recalling 316 cartons of Actiq 200 mcg fentanyl lozenges because they failed dissolution specifications during stability testing.
Linde Gas North America is recalling MEDICYL-e Portable Oxygen Systems because some units may have misapplied valve flow knobs.
Spartan Motors is recalling 2013 Gladiator and Metrostar emergency vehicles because electrical signal fluctuations may cause airbags or seat belt pretensioners to deploy inadvertently.
GE Healthcare is recalling PET VCAR software due to a potential safety issue with automated PERCIST response criteria calculations.
Gromex Inc. is recalling Gromex Camaron Entero (Whole Shrimp) because the product may contain undeclared bisulfites. The recall affects consumers in Connecticut, New Jersey, New York, and Pennsylvania.
Tecan US, Inc. is recalling 12 Freedom EVO instruments with Touch Tools Suite 3.0 because door lock errors are ignored, potentially causing unexpected movement and operator injury.
Biomet is recalling 75 Phoenix Retrograde Femoral Connecting Bolts because an undersized diameter may cause the hex driver to get stuck, delaying surgery.
Verathon is recalling GlideScope reusable laryngoscope blades because the tips may break prematurely without visible signs, posing a risk to patients during intubation.
Gromex Inc. is recalling Anelina (dried shrimp) because it contains undeclared bi-sulfites and unapproved colors. The product was distributed in Connecticut, New Jersey, New York, and Pennsylvania.
Ford is recalling 2013 Explorer, Taurus, and Lincoln MKS vehicles because child safety locks may deactivate without notice, posing a risk to unrestrained children.
Philips Healthcare is recalling 116 BuckyDiagnost radiographic systems because table height measurements were found out of specification, potentially causing system mis-alignment.
Oskri Corp. is recalling Sesame Bars Date Syrup because they may contain copper shavings. The recall affects 1,650 five-pack boxes distributed in Massachusetts.
Julian's Recipe is recalling specific lots of European Style Pretzel Baguettes due to an undeclared soy flour ingredient caused by a repacking error.
Zimmer, Inc. is recalling 344 Patient Helper Bed Frame Adapter Assemblies because they may have a weak weld where the mounting bars attach to the tube.
Nu Wa Industries is recalling one 2006 Hitchhiker Champagne Edition RV because power awning motor screws may shear, causing the awning to unfurl unexpectedly.
Farber Specialty Vehicles is recalling two vehicles equipped with Ricon wheelchair lifts because an armored cable may not clear the lift, posing a fire risk.
Synthes USA HQ, Inc. is recalling 10 units of 11-Hole, 1/3 Tubular Plate DCL Plates with Collar because they were released to the US market in error.
SybronEndo is recalling 3,615 Elements Obturation Units because a required Canadian safety caution label was accidentally omitted from the device and its power cord.
Siemens is recalling 8 ARTISTE linear accelerators due to potential image quality degradation that may affect patient position verification during cancer treatment.
Hi-Tech Pharmacal is recalling specific lots of HydrOXYzine Hydrochloride Oral Solution because the product failed stability testing and may be subpotent.
Bao Gong Da Inc is recalling American Ginseng products because FDA lab analysis found pesticide residues. The recall covers retail and bulk packages distributed in four states.
Coca-Cola is recalling specific Minute Maid Cranberry Apple Raspberry juice bottles due to potential spoilage or damage to the bottle lip.
Ortho-Clinical Diagnostics is recalling a specific lot of VITROS Chemistry Products-HCY Reagent because it produced lower than expected results.
Coca-Cola is recalling specific lots of Minute Maid Apple Juice because some bottles may have damaged lips or spoilage.
Coca-Cola is recalling Minute Maid Strawberry Passion juice bottles due to potential spoilage or damage to the bottle lip.
Coca-Cola is recalling specific lots of Minute Maid Orange Juice in 10oz and 15.2oz bottles due to potential spoilage or damage to the bottle lip.
Coca-Cola is recalling specific lots of Minute Maid Mixed Berry Juice because some bottles may have damaged lips or spoilage.
Aperio Technologies is recalling 364 ScanScope systems because user guides incorrectly claim FDA clearance for diagnostic use, when the devices are for research only.
SybronEndo is recalling 3,615 Elements Obturation Unit power cords because a required Canadian safety label was accidentally omitted from the packaging.
Hitachi is recalling 45 Echelon, Echelon Oval, and Oasis MR imaging systems due to a software error that can cause image data loss during simultaneous scanning and processing.
Prism Medical Services USA is recalling 5 BC Hammock Mesh Slings (Large) because they were produced in the incorrect size.
Prism Medical Services USA is recalling BC Hammock Mesh Sling (Junior) units because they were produced in the incorrect size.
Jus Made, Inc. is recalling 1,995 cases of Roo's Juice Tropical Orange Flavor due to potential contamination with bacterial biofilm, mold, and red water mites.
Pfizer is recalling specific lots of Norpace CR (disopyramide phosphate) capsules because they failed to meet dissolution specifications.
Philips Healthcare is recalling 177 stationary radiographic systems because their Installation Acceptance Test Documents were non-compliant with regulations or could not be located.
Philips Healthcare Inc. is recalling 101 units of Diagnost Stationary Radiographic Systems because installation records show table height measurements out of specification.
Mission Pharmacal Co is recalling 8,437 bottles of Sodium Sulfacetamide 10% and Sulfur 5% Lotion because the active ingredients were formulated too high.
Prism Medical Services USA is recalling 5 BC Hammock Mesh Sling units because they were produced in the incorrect size, failing to meet the firm's standards.
Faria Limited LLC is recalling Dr. Sheffield's Triple Antibiotic Ointment because it failed stability specifications and could not meet shelf-life requirements.
Philips Healthcare Inc. is recalling 66 BuckyDiagnost Radiographic X-ray systems because installation acceptance test documentation was missing or inconsistent.
Prism Medical Services USA is recalling 10 BC Hammock Mesh Slings (Medium) because they were produced in the incorrect size.
IDEV Technologies is recalling three SUPERA VERITAS stents because of an error on the outer labeling. The inner label was correct.
EverGreen is recalling 2010-2012 Ever-Lite and Element travel trailers because propane cylinders may leak or rupture, posing a fire risk.
Bel Air Lighting is recalling about 20,500 nine-light chandeliers because the mounting loop can break, causing the fixture to fall and pose an impact injury hazard.
Genlyte is recalling about 80,300 Capri track lighting fixtures because they can fall off the track rail, posing an impact injury hazard to bystanders.
Horizon Hobby is recalling Dynamite 7.4V LiPo batteries used in Losi Micro remote control vehicles because incorrect wiring can cause overheating and fire.
Thor Motor Coach is recalling specific model years of Windsport, Magellan, Hurricane, Serrano, and A.C.E. motorhomes because a battery control center may fail while driving, causing total power loss and increasing crash risk.
Hyundai is recalling 2012-2013 Azera vehicles because the occupant detection system may fail to correctly identify the front passenger, potentially causing the airbag to deploy with incorrect force.
Brammo is recalling 87 model year 2013 Empulse motorcycles because the rear tail assembly bracket can fatigue and break off, increasing crash risk.
Honda is re-recalling 2007-2008 Fit vehicles because water intrusion can damage the power window switch, potentially causing overheating, smoke, and fire.
Turtle Top is recalling certain 2007-2012 Ford Odyssey, Terra Transport, and Van Terra vehicles equipped with Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.
Sutrak USA is recalling HVAC systems used in DART 39000 buses because a fuse holder defect may allow voltage spikes that damage electrical components and cause a fire.
Vermeer is recalling 2012-2013 R9X12T trailers because an incorrectly installed air-brake booster valve may increase stopping distances, raising the risk of a crash.
Mobility Works is recalling 2006-2012 Ford E-150, E-250, and E-350 vans equipped with specific wheelchair lifts due to a potential fire hazard from cable contact.
Elkhart Coach is recalling 2006-2012 shuttle buses because a wheelchair lift cable may cause a short circuit and fire.
North American Bus Industries is recalling 2012-2013 transit buses due to a fuse holder defect that may cause voltage spikes and electrical fires.
Mitsubishi is recalling 2011 Outlander Sport vehicles because the panoramic glass roof may have been installed without primer, potentially allowing it to detach.
Zero Motorcycles is recalling 2013 FX and XU motorcycles because a battery sealant defect may allow water penetration, potentially causing burns.
Kichler Lighting is recalling Aztec chandeliers sold at Lowe's because the fixture loop can fail, causing the light to fall from the ceiling.
Collins Bus is recalling 17 model year 2006-2007 Mid Bus CSD-7450R-C vehicles because a wheelchair lift cable may cause a short circuit and fire.
Paddywax is recalling about 2,100 fragrance diffusers because their labels omit petroleum distillates, a substance that poses an aspiration hazard if swallowed.
Advance Pharmaceutical Inc. is recalling Rugby Natural Iron Supplement bottles that contain Meclizine HCl instead of ferrous sulfate due to a label mixup.
Olaax International is recalling MAXILOSS Weight Advanced capsules because they contain sibutramine, an unapproved drug removed from the U.S. market for safety reasons.
Fruit Treasure Inc is recalling fresh Thai chili peppers because FDA testing found Salmonella. The peppers were distributed within California.
Trophy Nut Co Inc is recalling specific nut products because they were made with pistachios that may be contaminated with Salmonella.
Trophy Nut Co Inc is recalling America's Choice 9 oz. Giant Pistachios because they were made with pistachios that may be contaminated with Salmonella.
Trophy Nut Co Inc is recalling Wa Wa brand 6 oz. Pistachio Gusset because it may be contaminated with Salmonella.
Rio Queen Citrus, Inc. is recalling 840 cartons of Karol brand Mexican cherry tomatoes due to potential Salmonella contamination.
Sandoz Inc. is recalling Cefazolin for Injection, USP 1 gm vials, lot DB2208, due to a lack of assurance of sterility caused by broken or cracked vials.
Isuzu is recalling specific 2001-2013 trucks because debris on the oil pan heater extension cord can cause overheating and fire.
Best Buy is recalling ATG replacement batteries for MacBook Pro computers because they can catch fire while charging, posing fire and burn risks.
Chrysler is recalling 1993-1998 Jeep Grand Cherokee and 2002-2007 Jeep Liberty vehicles because fuel tanks may leak in rear impacts, posing a fire risk.
Trophy Nut Co Inc is recalling specific Red Pistachio Tubes because they were made with pistachios potentially contaminated with Salmonella.
Ohlins is recalling steering dampers for BMW motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock and leading to injury or a crash.
Blessing Seafood is voluntarily recalling specific lots of Wild White EZ Peel Shrimp due to undeclared sulfites. The product was sold at Hy-Vee stores and one fish market.
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