Archive
445 recalls were announced in July 2012.
Of the 445 recalls this month scored against our rubric, 3% are Critical, 21% are Severe.
Which agencies issued them
Dutchmen is recalling 2013 Coleman and Dutchmen travel trailers because the propane line may be damaged by the rear axle, posing a fire or explosion risk.
Cottrell is recalling 2006-2011 trailers with Meritor axles because low bearing durability can cause wheel end fires. Owners should contact Meritor for free repairs.
Newmar is recalling 2008-2009 Grand Star Class A motorhomes because brake caliper pistons may grow, causing drag and reduced braking performance.
Liberty Mountain is recalling VAUDE Kenta and Kenta Plus child carriers because a side strap seam can unravel, posing a fall hazard to children.
Green Toys is recalling approximately 52,500 mini vehicles sold in the U.S. and Canada because wheels and hubcaps can detach, posing a choking hazard to young children.
Keystone RV Company is recalling 220 model year 2013 Bullet Premier 31BHPR travel trailers due to incorrect information on federal identification and tire loading labels.
Gulf Stream is recalling 443 Class A motor homes from 2006-2008 because brake caliper pistons may grow, causing drag and reduced braking performance.
Keystone RV Company is recalling 117 model year 2013 Outback and Sydney recreational vehicles manufactured in July 2012 that may lack a smoke detector.
Thor Industries is recalling 2013 Crossroads Cruiser recreational trailers because incorrect information on federal identification and tire labels may lead to improper loading and tire failure.
ZAP is recalling 2008 Xebra motorcycles because they lack separate brake fluid reservoirs, which could compromise braking ability and increase crash risk.
Mazda is recalling 2001-2006 and 2008 Tribute vehicles because a stuck throttle could cause a crash, serious injury, or death.
NHTSA recalls 2012 Rolls-Royce Ghost vehicles because the tire label incorrectly lists 19-inch tires instead of the installed 20-inch tires.
Ford is recalling 2001-2004 Escapes with 3.0L V6 engines because inadequate clearance between the engine cover and speed control cable could cause a stuck throttle, leading to high speeds and potential crashes.
Keystone RV Company is recalling 2010-2012 Cougar models because the rear bumper holding the spare tire may fail due to metal fatigue.
HeathCo is recalling about 7,800 Motion Security Lights sold at Home Depot because internal wiring can be damaged, posing an electrical shock hazard.
Etac Supply Center Ab is recalling Ono, Avant, and Salsa walkers because wheels may fall off, posing a risk of serious injury or death.
Hospira Inc. is recalling Morphine Sulfate Injection cartridges that contain 2.2 mL instead of the labeled 1 mL, posing a risk of overdose.
Luitpold Pharmaceuticals is recalling Epinephrine Injection ampules because of the presence of particulate matter. The affected lot was distributed nationwide.
Blue Bird is recalling 2013 Vision and All American non-school buses because driver's seat belts may have mismatched buckles that fail to engage properly.
Standard Process, Inc. is voluntarily recalling 12,422 bottles of Pancreatrophin PMG dietary supplements due to potential Salmonella contamination.
Old Fashioned Foods, Inc. is recalling Zesty Bean Dip and Jalapeno Bean Dip due to inadequate processing under acidified food regulations.
Thor Industries is recalling 2010-2013 Breckenridge travel trailers because a defective furnace gas valve can stick open, potentially causing a gas leak and fire.
Hyundai is recalling 2007-2009 Santa Fe vehicles because the occupant classification system may fail to detect small adults, potentially preventing the front passenger airbag from deploying.
Hitachi is recalling Scenaria CT System software due to a defect that may cause incomplete image reconstruction, potentially resulting in missing diagnostic data.
Terumo is recalling 648 Advanced Perfusion System 1 units due to a Red X error indicating loss or fluctuation of internal power on one side of the base.
Epocal Inc is recalling 8,650 epoc Blood Analysis BGEM Test Cards because a portion of the lot may report inaccurate low glucose results.
Terumo is recalling 81 Sarns Modular Perfusion System 8000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Philips Medical Systems is recalling 524 Brilliance CT scanners because defective bolts securing the carbon table top may break off.
Terumo is recalling 484 Sarns Modular Perfusion System 9000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Blue Bird is recalling 726 model year 2013 All American and Vision school buses because driver's seat belts may have mismatched buckles that fail to engage properly.
Terumo Cardiovascular Systems is recalling 286 Sarns Modular Perfusion System 9000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Truitt Bros. Inc. is recalling 95 cans of Pacific Northwest Premium Navy Beans due to undeclared soy. The product was distributed to California, Oregon, and Washington.
Kimberly-Clark is recalling specific lots of MicroCool surgical gowns because they pill, lint, or allow blood to pass through.
Terumo is recalling 310 Sarns Modular Perfusion System 8000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Terumo is recalling 461 Sarns Modular Perfusion System 8000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Terumo is recalling 648 Advanced Perfusion System 1 units due to reports of communications or power failures in the system network.
Standard Process is voluntarily recalling Cataplex C dietary supplements due to potential Salmonella contamination. Consumers should stop using the affected products.
Terumo is recalling 992 Advanced Perfusion System I units worldwide due to reported malfunctions in the Air Bubble Detection System, including oversensitivity and false alarms.
Spacelabs Healthcare is recalling 21 Xprezzon Bedside Monitors because specific key presses can cause patient parameters to disappear from the display.
Terumo is recalling 26 Sarns Modular Perfusion System 8000 units due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Alere San Diego is recalling 9,997 Triage Tox+MTD Drug Screen kits because they may produce false positive or negative results due to decreased precision and accuracy.
Nutri-Health Supplements is recalling iFlora Kids Multi-Probiotic because a supplier notified them that the galactooligosaccharide ingredient used in the product was recalled for suspected salmonella contamination.
GE OEC recalled 726 OEC 9900 Elite C-arm systems worldwide due to a defective vertical lift column power supply identified during an FDA inspection.
Kimberly-Clark is recalling specific lots of MicroCool surgical gowns because they pill, lint, or allow blood strikethrough, potentially compromising sterility.
EKOS Corporation is recalling EkoSonic MACH4 Endovascular Devices because radio-opaque marker bands may dislodge and the MicroSonic Device may break during use.
Stryker is recalling 532 units of T2 Knee Arthrodesis Nails because of a potential breach in the sterile packaging barrier.
Varian is recalling Eclipse Treatment Planning Systems because changing dose prescriptions in certain plans may result in incorrect Monitor Units and dose distributions.
CareFusion 203, Inc. is recalling 266 EnVe Ventilators because they may fail to hold set pressure values or alarm for circuit faults, potentially compromising patient ventilation.
Micro Bird is recalling 2011-2012 G5 school buses because roof escape hatches may be too hard to open, potentially hindering emergency egress.
Terumo Cardiovascular Systems is recalling 274 Sarns Modular Perfusion System 8000 units due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Terumo is recalling 31 Sarns Modular Perfusion System 9000 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
GE Healthcare is recalling 279 invasive blood pressure care cables due to a faulty O-ring that prevents correct blood pressure monitoring.
Teleflex Medical is recalling Hudson RCI Concha Therm Neptune Humidifiers because a speaker failure could prevent audio alarms from sounding, potentially delaying patient treatment.
Terumo is recalling Sarns Modular Perfusion System 8000 units due to reported malfunctions in the Air Bubble Detection System, including false alarms and over-sensitivity.
Eldorado is recalling 2,215 model year 2007-2011 buses because wheelchair lift latches may bend, posing a fall risk to occupants.
SunOpta Ingredients Group is voluntarily withdrawing specific lots of Canadian Harvest Oat Fiber 300-33 due to possible contamination with Cronobacter sakazakii.
Terumo is recalling 992 Advanced Perfusion System 1 units due to a power loss error message that may affect system stability during medical procedures.
Standard Process, Inc. is voluntarily recalling Cataplex ACP dietary supplements due to potential Salmonella contamination.
Michelin North America is recalling specific BF Goodrich and Uniroyal tires due to a risk of tread/belt separation that could cause rapid air loss and increase crash risk.
Terumo is recalling 648 Advanced Perfusion System 1 units worldwide due to reported malfunctions in the Air Bubble Detection System, including false alarms and oversensitivity.
GE OEC Medical Systems is recalling OEC 9800 series motorized C-arm systems because a defective vertical lift column power supply is subject to early life failure.
Terumo is recalling 992 Advanced Perfusion System 1 units worldwide due to reports of communications and power failures in the system network.
LMA North America Inc is recalling 18,799 units of the LMA Esophageal Intubation Detector (EID100) because the device may produce false positive results during intubation confirmation.
Stryker Spine is recalling AVS Navigator Trials because the shaft may fail at the junction of the trial head.
GE OEC Medical Systems is recalling OEC 8800 Flexiview imaging devices because an FDA inspection found a defective vertical lift column power supply subject to early life failure.
B. Braun Medical is recalling 38,225 Infusomat Space Pumps because the anti-free flow clip catch may break if the IV set is inserted incorrectly.
Old Fashioned Foods is recalling Jalapeno Bean Dip because it was not processed according to FDA regulations for acidified foods.
Meda Pharmaceuticals is recalling Prefera OB One Gel Capsules because the product labeling failed to list several inactive ingredients, including D&C Red #33.
Stingray Surgical Products is recalling bipolar forceps because the Instructions For Use were altered without FDA clearance.
Abbott Molecular is recalling the Bar Code Scanner User's Guide because incorrect bar codes may prevent proper language configuration of the scanner.
Becton Dickinson is recalling Gram Crystal Violet 250 mL reagents due to potential artifacts that may interfere with the identification of microorganisms.
Gulf Fiberoptics, Inc. is recalling 169 GMF-RC65 Replacement Surgical Headlight Cables because the light-transmitting fiber material differs from the approved 510(k) design.
GE Healthcare is recalling Optima XR200 and XR220 mobile X-ray systems because a software issue affects the visual indication required by regulations.
Critical Diagnostics is recalling Presage ST2 Assay kits because they may produce inaccurate test results for patients with chronic heart failure.
DeRoyal Industries is recalling 303 custom surgical kits and trays because clear protective tape was not applied during manufacturing.
Becton Dickinson is recalling 539 BD Gram Stain Kits because increased artifacts may interfere with the distinction between microorganisms.
Integra Limited is recalling 108 Take-Apart Endoscopic Instruments because internal shaft components were out of specification.
Pack Pharmaceuticals is voluntarily recalling 4,848 bottles of Ciprofloxacin 500 mg tablets because two bottles were found missing container labels.
JHP Pharmaceuticals is recalling specific lots of Pitocin (Oxytocin) injection due to a labeling error that displays an incorrect lower storage temperature limit.
Sigma issued a safety alert for the SIGMASpectrum Infusion Pump Master Drug Library Editor software because it may create drug libraries that do not reflect common clinical practices.
Bayer is recalling 119,412 cartons of Midol Complete because the blister strip label does not match the carton regarding the maximum daily dose.
Vintage Pharmaceuticals is recalling 73,746 bottles of Hydroxyzine Hydrochloride Oral Solution because high levels of a known impurity were detected.
Bayer Healthcare is recalling 48,528 cartons of Midol Complete because the maximum daily dose stated on the blister strip does not match the carton label.
Peg Perego is recalling Venezia and Pliko-P3 strollers because infants can become entrapped between the seat and tray, posing a strangulation hazard.
Daimler Trucks North America is recalling two 2013 Thomas Built Saf-T-Liner C2 school buses due to a front axle machining error that could cause wheel separation and loss of control.
Crossroads is recalling 2010-2011 Hampton travel trailers because a defective furnace gas valve may stick open, causing a gas leak and potential fire.
Kolcraft is recalling about 5,600 Contours Options LT tandem strollers because the front wheel assembly can break or nuts can detach, posing fall and choking risks.
Blue Bird is recalling 19 model year 2013 Vision school buses because a missing electronic module may prevent the brake pressure warning light from activating.
Hyundai is recalling 2012-2013 Sonata vehicles because the curtain side airbags may inflate without a deployment command, increasing the risk of injury and driver distraction.
Jayco is recalling specific 2007-2011 motorhomes and fifth wheels because an improper electrical connection could cause overheating and fire.
Elkhart Coach is recalling 2011 transit buses because roof escape hatches may not open easily in an emergency, increasing injury risk.
Kawasaki is recalling 2008-2012 Concours 14 motorcycles because debris can trap in the brake pedal, causing rear brake overheating, lock-up, or failure.
Collins is recalling 171 model year 2012 school buses because clothing or backpack drawstrings can get caught in the open door, potentially pulling passengers under the vehicle.
Collins Bus Corporation is recalling 1,429 model year 2012 school and multi-function buses because emergency egress windows may fail to meet federal safety standards.
Navistar is recalling specific 2010-2011 International Lonestar trucks because the wheels may crack and separate, potentially causing a crash.
Idle Free Systems is recalling certain aftermarket auxiliary power units for heavy trucks due to a potential fire risk from a battery separator defect.
Collins Bus Corporation is recalling 196 model year 2012 school and activity buses because the electrical panel cover may not be secured, posing a risk of falling and distracting the driver.
Club Car is recalling about 800 gas-powered golf and transport vehicles because the fuel hose can separate from the tank, posing a fire hazard.
Double K is recalling 2007-2009 Hometown Trolley vehicles because wheelchair lift latches may bend, risking occupant falls.
Collins Bus Corporation is recalling 598 model year 2012 school and activity buses because the fuel filler hose may be damaged by seat bolts, creating a fire risk.
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