Archive
337 recalls were announced in October 2017.
Of the 337 recalls this month scored against our rubric, 3% are Critical, 28% are Severe.
Which agencies issued them
USDA issued a public health alert for Trader Joe's broccoli slaw and kale salads with chicken due to possible Listeria contamination.
KZRV is recalling 2017-2018 Connect recreational trailers with outside kitchens because the 110-volt outlet lacks Ground Fault Circuit Interrupter (GFCI) protection, posing a shock risk.
Polaris is recalling about 19,000 General side-by-side vehicles because the steering wheel shaft can shift and detach, creating a crash risk.
BMW is recalling 740,561 vehicles from 2007-2011 because a short circuit in the PCV valve heater can cause a fire.
Mitsubishi is recalling 2014-2018 Mirage vehicles because the air bag system may disable itself due to sensor errors, increasing injury risk.
Motor Coach Industries is recalling 2018 MCI J4500 buses because air lines were incorrectly hooked to pressure gauges, potentially delaying driver response to low air conditions.
Taylor Farms Florida is recalling approximately 732 pounds of chicken salads because they contain undeclared anchovies, a known allergen.
Arctic Cat is recalling specific Wildcat Trail and Sport models because heat from the exhaust can melt plastic panels, posing a fire hazard.
East Manufacturing is recalling 2013-2018 Frameless Dump Hybrid trailers because draft arm tubing may crack and fail, potentially causing loss of vehicle control.
Eldorado is recalling 2017 Axess, Arrivo, XHF, and E-Z Rider II buses because seat belt buckles may be stuck, preventing use.
Indian Motorcycle is recalling 2,096 models from 2017-2018 because some may have European-market headlights that fail US safety standards, increasing crash risk.
Forest River is recalling 2017-2018 Rockwood and Flagstaff travel trailers because the slide room arm may damage the rear tire, increasing crash risk.
Tremcar is recalling specific Hutchinson and Tremcar trailers because their rear impact guards were made with insufficiently strong aluminum alloy.
Jaguar Land Rover is recalling 2017 Range Rover and Range Rover Sport vehicles because the instrument cluster may intermittently go blank, increasing crash risk.
Jaguar is recalling 2016-2018 XF, F-Pace, XJ, and XE vehicles because the instrument cluster may go blank, increasing crash risk.
Honda is recalling 2,443 2017 CBR1000RR and CBR1000RR SP motorcycles because a gap in the fuel tank cap seal may allow water to enter the tank, potentially causing engine stalling and increasing crash risk.
The Kroger Co is recalling 2,634 Chicken Salad Sandwiches contaminated with Listeria monocytogenes. The product was distributed in Colorado, New Mexico, Utah, and Wyoming.
Deserving Health International Corp is recalling Symbio Muc Eye eye drops because the product lacks assurance of sterility. The affected units were distributed throughout the United States.
RXQ Compounding LLC is recalling 945 vials of methylprednisolone acetate injection because autoclave parameters were incorrect, raising concerns about product sterility.
Death Wish Coffee Company is recalling 80,777 cans of Nitro Canned Cold Brew Coffee nationwide due to a potential for Clostridium Botulinum.
Keystone is recalling 2017-2018 Cougar western edition trailers because stabilizer jacks may detach during transit, creating a road hazard.
BMW is recalling 2006-2011 3 Series vehicles because heating and air conditioning wiring may overheat, increasing the risk of a fire.
Dean Foods is recalling 1,804 gallons of Tampico Tropical Punch in 1-gallon jugs due to undeclared milk. The product was distributed in Wisconsin, Illinois, and Indiana.
The Harvard Drug Group is recalling Alprazolam Tablets, 0.25 mg, due to an out-of-specification result for an unknown impurity.
Hong Lee Trading is recalling Vina Cafe Wake-Up Instant Coffee Mix because it contains undeclared milk. The product was distributed in New York, New Jersey, and Connecticut.
St Jude Medical is recalling 164,366 Assurity MRI pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
Medtronic is recalling 423 VCLAS laser applicator systems because they were not appropriately tested for saline leakage during manufacturing.
Bel Brands USA is recalling Merkts Port Wine Cheese Spread after customers reported finding white plastic pieces in the product.
St Jude Medical is recalling 101 implantable pacemaker pulse generators to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
St Jude Medical is recalling 6,051 PM 1260 Assurity+ pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
St. Jude Medical is recalling 28,817 Proclaim 5 and 7 Elite Implantable Pulse Generators because battery longevity estimations may be inaccurate.
St Jude Medical is recalling specific Assurity and Accent pacemaker models to mitigate the risk of unauthorized access via radio frequency communications.
St. Jude Medical is recalling 3,119 Infinity 5 and 7 Implantable Pulse Generators because battery longevity estimations may be inaccurate.
St Jude Medical is recalling 2,726 implantable pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
St Jude Medical is recalling 2,741 Nuance pacemakers to install new firmware that mitigates the risk of unauthorized access to the devices' radio frequency communications.
St Jude Medical is recalling specific Anthem and Allure/Relieve pacemakers to mitigate the risk of unauthorized access via radio frequency communications.
CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of increased or decreased medication flows.
Volkswagen Group of America is recalling 2017-2018 Audi A4 and A5 vehicles because loose aluminum door trim can expose sharp edges, increasing the risk of injury to occupants.
PlanToys is recalling about 500 baby gyms sold in 2016 and 2017 because babies can strangle on the side rope crossbars. No injuries have been reported.
USDA FSIS issued a public health alert for Mary's Harvest kale and broccoli slaw salad with chicken due to possible Listeria contamination from a recalled broccoli supplier.
St. Jude Medical is recalling 10,453 Merlin PCS 3650 programmers worldwide to install new firmware that mitigates the risk of unauthorized access to pacemakers.
St. Jude Medical is recalling 1,744 Proclaim DRG Implantable Pulse Generators because the battery indicator status may be inaccurate.
St Jude Medical is recalling 4,828 ZENEX pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
La Terra Fina is recalling Spinach Artichoke & Parmesan Dip & Spread because it contains an undeclared egg allergen. The product was distributed in 11 U.S. states.
Genesys Orthopedics is recalling 120 Binary Screwdrivers because the threaded inner shaft tip can break off during cervical screw insertion.
St. Jude Medical is recalling Merlin@Home software to mitigate the risk of unauthorized access to pacemakers using radio frequency communications.
Diving Unlimited International is recalling approximately 480 scuba diving regulators because they can malfunction, posing a drowning hazard. No injuries have been reported.
Philips is recalling Brilliance iCT SP CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.
Cepheid is recalling Xpert EV Assay kits because customers reported a higher than expected number of invalid test results.
Philips Electronics North America Corporation is recalling 606 Brilliance 64 CT systems in the US because a software defect prevents image reconstruction after certain scans.
Philips is recalling Ingenuity CT systems because a software defect prevents image generation during bolus tracking procedures, potentially requiring patient rescans.
Philips is recalling Brilliance iCT CT scanners because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.
Philips is recalling Ingenuity Core128 CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patient rescans.
Teleflex Medical is recalling Pilling Knife Handles because the slot depth is out of specification, which may prevent blades from fitting properly.
Unichem Pharmaceuticals is recalling 96,876 bottles of Bisoprolol Fumarate 5 mg tablets because stability testing revealed an out-of-specification unknown impurity.
Toshiba American Medical Systems Inc is recalling 96 Kalare Fluoroscopic X-Ray Systems because images may fail to display on the system monitor or save to the hard disk.
Hologic is recalling one Panther System unit in Indiana because an incorrect incubator was installed, which may have led to incorrect Aptima Combo 2 assay results.
Philips is recalling 606 Ingenuity Core CT systems in the US because a software defect prevents image reconstruction after bolus tracking scans.
Chrysler is recalling 2018 Jeep Cherokee and Compass vehicles with 2.4L engines due to a cracked oil pump housing that can cause engine stalling and increase crash risk.
Ford is recalling 2017 F-150 trucks with ten-speed transmissions because a pin may detach, causing the vehicle to roll or fail to move as selected.
Fisher-Price is recalling Soothing Motions Seats because the motor housing can overheat, posing a fire hazard. No injuries have been reported.
Silverstone is recalling Ride Eazy Trimless helmets in sizes S through XXL because they may not adequately protect wearers in a crash, failing to meet federal safety standards.
Ford is recalling 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.
Ford is recalling 2018 F-150 trucks with 3.5L engines because cylinder heads may lack lubrication holes, risking engine failure and crashes.
Ford is recalling 2018 F-150 trucks with 3.3L engines and column shift levers because quickly moving the lever may cause unintended gear selection, increasing crash risk.
Fresh Foods Manufacturing Co. is recalling approximately 701 pounds of heat-treated chicken products that may be contaminated with Listeria monocytogenes.
BSH Home Appliances is expanding a recall of approximately 408,000 dishwashers due to a fire hazard caused by overheating power cords. No injuries have been reported, but five property damage incidents have occurred.
Aperia Technologies is recalling Halo Tire Inflators because adapter plate brackets may crack, causing rapid tire deflation and increased crash risk.
Walter Kidde is recalling specific fire extinguisher models that may clog or have nozzles detach, potentially causing injury or failure during a fire.
Keystone is recalling specific 2017-2018 Crossroads recreational vehicles because the outdoor cook top's fiber board can burn if flames invert, creating a fire hazard.
Daimler Trucks North America is recalling 2012-2018 Thomas Built Buses Saf-T-Liner C2 school buses because propane fuel lines may contact the transmission yoke, potentially causing a leak and fire.
General Motors is recalling 2011-2015 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks because a stuck fuel sensor may cause the front tank to overfill, potentially leading to a fuel leak and fire.
Accessible Technologies is recalling ProCharger Superchargers for 2012-2017 Jeep Grand Cherokee SRT vehicles because the mounting bracket may damage the ABS line, causing a brake fluid leak.
Kids Preferred is recalling about 587,000 wind-up musical plush toys because the metal wind-up mechanism can detach, posing a choking hazard to young children.
Van-Con is recalling 2011-2017 Dual Rear-Wheel school buses because seat belt buckles may rest across passengers' laps, increasing injury risk in crashes.
Allen's Blueberry Freezer, Inc. is recalling 30-lb boxes of IQF Wild Blueberries because the product tested positive for Listeria monocytogenes.
United Pharmacy is recalling 268 vials of compounded Glutamine, Arginine, and Carnitine injection due to CGMP deviations and the absence of glutamine.
Navistar is recalling 2016-2017 IC Bus school buses because the seat belt buckle mount rod can fracture under load, increasing injury risk in a crash.
Toyota is recalling 2005-2007 and 2009-2010 Sienna vehicles because the shift lever may move out of Park without depressing the brake pedal, increasing crash risk.
Navistar is recalling 778 school buses because air brake hoses may contact tires, potentially causing brake failure or increased stopping distance.
Nissan is recalling 2016-2017 Rogue vehicles because improper welds on rear seat recliner joints may increase injury risk in a crash.
Toyota is recalling 2016 Prius vehicles because a capacitor in the hybrid system may not be properly secured, which could cause a loss of motive power and increase crash risk.
Navistar is recalling 2015-2018 IC Bus RE commercial buses because air brake hoses may contact tires, potentially causing brake failure or increased stopping distance.
Les Chateaux De France is recalling bacon-wrapped scallops because they contain undeclared milk and are misbranded. The products were shipped to institutional locations in five states.
Taylor Farms New Jersey is recalling Wawa Fruit & Cheese products because an ingredient may contain wood slivers. The recall covers 36,177 units distributed to several states.
Pinnacle Food Group is recalling Birds Eye Baby Sweet Peas due to potential Listeria monocytogenes contamination. Consumers should check their freezers for the affected lots.
Volkswagen is recalling 2018 Tiguans because the back-up lights may not be bright enough, increasing the risk of a crash.
Handicare is recalling 8 A-Series patient lifts because the lift straps may wear prematurely at maximum load, posing a risk of patient drop.
Tai Foong USA Inc is recalling Royal Asia Shrimp Wonton Noodle Soup sold at Costco due to undeclared egg, a major food allergen.
Abbott is recalling 1,385 ARCHITECT c4000 cuvette segments because a detached post may cause falsely depressed patient results in adjacent cuvettes.
Handicare AB is recalling nine Carina mobile lifts because they were delivered with locking pins that are too small. This defect may cause increased wear on internal components.
Silver Spring Foods is recalling Waterfront Bistro Tartar Sauce because the label fails to identify egg as an ingredient.
St Jude Medical is recalling approximately 90,563 Fortify and Fortify Assura implantable cardioverter defibrillators because they may exhibit premature battery depletion.
St Jude Medical is recalling specific Unify and Quadra Assura cardiac resynchronization therapy defibrillators because they may exhibit premature battery depletion.
First Source is recalling Bristol Farms Tasty Treats Nonpareils Milk Chocolate because the ingredient label incorrectly omits milk, posing a risk to consumers with milk allergies.
Apple King, LLC is recalling Nature's Delight brand Fuji apples because the pesticide Thiabendazole was detected at 6.9 ppm.
Cargill Salt is recalling 800 cases of Sea Salt Tablets due to equipment malfunction that introduced small metallic fragments and particulate matter.
Dr. Reddy's is recalling specific lots of famotidine tablets sold as CVS Pharmacy Acid Controller and Equate Famotidine due to an out-of-specification impurity result.
Boehringer Ingelheim is recalling 128 bottles of Mobic 15 mg tablets because they were packaged with an incorrect insert.
GB Green Gastronome is recalling approximately 8,000 pounds of chicken and pork steam buns because they contain undeclared coconut milk and cream, which are tree nut allergens.
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