Archive
559 recalls were announced in March 2015.
Of the 559 recalls this month scored against our rubric, 18% are Critical, 26% are Severe.
Which agencies issued them
Mercedes-Benz USA is recalling 2014-2015 Smart Fortwo vehicles because steering gear mounting bolts may break, increasing crash risk.
BMW is recalling 18,054 vehicles due to a fuel pump defect that may cause the vehicle to stall without warning, increasing crash risk.
Thor Motor Coach is recalling 2015 Siesta and Citation motorhomes because an incorrectly installed door component may make doors harder to open after a crash.
Bauer Hockey is recalling specific goalie masks and replacement wire cages because the metal wires can break, posing a risk of facial impact or laceration.
Blinds To Go is recalling about 200,000 custom-made window shades because the cord hold-down device can fail, posing a strangulation risk to small children.
Buy4easy is recalling TMS JX-A5005 full-face helmets because they failed penetration tests and do not meet DOT regulations.
BMW is recalling certain 2013-2014 5 Series vehicles because rear reflex reflectors may not reflect enough light, increasing crash risk.
Airstream is recalling 2015 Interstate motorhomes because an incorrectly installed door component may make doors harder to open after a severe frontal crash.
Giant Factories is recalling approximately 240 gas water heaters because a failing flame arrestor poses a risk of fire or explosion if flammable materials are nearby.
Daimler Trucks North America is recalling 3,732 model year 2015 Freightliner and Western Star trucks because improperly seated brake chamber diaphragms may cause brake drag and loss of vehicle control.
Ohlins is recalling TTX36 aftermarket motorcycle shock absorbers because the damper rod nut may loosen, potentially causing loss of vehicle control.
MCI is recalling 2014-2015 motor coaches because improperly torqued tie rod nuts may cause loss of vehicle control and increase crash risk.
Motor Coach Industries is recalling 2007-2010 MCI E4500 and J4500 motor coaches because a seat tether bar may interfere with the driver's seat belt locking mechanism.
Forest River is recalling 2015 Coachmen Prism RVs because an incorrectly installed door component may make doors harder to open after a crash.
Crossroads is recalling 2016 model year recreational trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.
Blue Bird is recalling 2,663 Vision school buses because a faulty voltage inverter may produce smoke and increase the risk of a fire.
Fiat is recalling 2013-2015 500E electric vehicles because incompatible software may cause the electric propulsion system to shut down, increasing crash risk.
Chrysler is recalling 2013-2014 Dodge Vipers because moisture in the door switch may cause doors to open unexpectedly while driving, increasing crash risk.
Blue Bird is recalling 2015-2016 Vision non-school transit buses because a voltage inverter failure may produce smoke and increase the risk of a fire.
Daimler Trucks North America is recalling 2014-2015 Western Star trucks equipped with certain Kidde fire extinguishers that may not fully discharge.
Lands' End is recalling about 173,000 children's pajamas and robes because they fail to meet federal flammability standards, posing a risk of burn injuries.
Kalmar is recalling 2014-2015 Ottawa T2 terminal tractors because incorrect ABS wiring can cause vehicle instability during braking, increasing crash risk.
Specialized Bicycle Components is recalling about 8,300 Aerobars because the mounting bolt can loosen, posing a fall hazard to riders.
Twin City Bagel, Inc. is recalling blueberry bagels sold under multiple brands because they may contain undeclared peanuts or almonds.
Twin City Bagel, Inc. is recalling Lender's Cinnamon Raisin Swirl bagels because they may contain undeclared peanuts or almonds.
Twin City Bagel, Inc. is recalling Essential Everyday Honey Wheat Bagels because they may contain undeclared peanuts or almonds.
Korean Food Co. is recalling Go hyang Mak Kimchi in 32 oz and half-gallon sizes because the product contains undeclared shellfish (shrimp).
Twin City Bagel, Inc. is recalling specific Jewel and Thomas onion bagels because they may contain undeclared peanuts or almonds.
Twin City Bagel, Inc. is recalling Pepperidge Farm Brown Sugar Cinnamon Mini bagels because they may contain undeclared peanuts or almonds.
Mutual Pharmaceutical is recalling Ergoloid Mesylates 1 mg tablets because they failed impurity and degradation specifications during stability testing.
Twin City Bagel, Inc. is recalling specific brands of whole wheat bagels because they may contain undeclared peanuts or almonds.
Twin City Bagel, Inc. is recalling specific Cinnamon Raisin bagels because they may contain undeclared peanuts or almonds.
Acme Smoked Fish Corp. is recalling Smoked Nova Salmon after Listeria monocytogenes was detected. The product was distributed in Virginia, Delaware, Maryland, and D.C.
Twin City Bagel, Inc. is recalling Kroger Cinnamon Swirl Raisin Bagels because they may contain undeclared peanuts or almonds.
Hospira is recalling 94,440 bags of 5% Dextrose Injection due to a potential leak at the administrative port that compromises sterility.
Pierce Manufacturing is recalling 2015 Saber, Enforcer, Impel, and Velocity vehicles because the rear leaf spring spacer block may crack, posing a crash risk.
Siemens is recalling 87 LANTIS Oncology Information System servers because using unvalidated operating systems may lead to incorrect patient treatment.
Heritage Pharmaceuticals is recalling RIFAMPIN for Injection, USP, 600 mg per vial, due to quality control concerns regarding the assurance of sterility.
Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.
Twin City Bagel, Inc. is recalling Dan's Pantry Wheat Bagels because they may contain undeclared peanuts or almonds.
Jack and the Beanstalk soybean and natto sprouts are being recalled in California due to positive FDA sampling for Listeria monocytogenes.
Heritage Pharmaceuticals is recalling Colistimethate Sodium Injection due to quality control concerns regarding sterility assurance.
Yamaha is recalling 4,900 model year 2015 motorcycles because a defective shift cam stopper may fracture, causing transmission shifting issues and increasing crash risk.
Twin City Bagel, Inc. is recalling plain bagels sold under multiple brand names because they may contain undeclared peanuts or almonds.
Tovli, Inc. is recalling Vegi-Chef Potato Knishes because they contain undeclared Yellow #5, a food dye.
Rill Foods is recalling Buena Mexi Chicken Chowder because the cumin used may be contaminated with peanut protein.
Chris A Papas & Son Co is recalling Dark Opera Cream eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Medtronic is recalling 151 FlexCath Select Steerable Sheaths because clinicians observed debris originating from the hemostasis valve outside of patients' bodies.
Chris A Papas & Son Co is recalling 4,968 French Cream eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Rill Foods is recalling Mount Mazama Lentil Chili because the cumin used may contain peanut protein. Consumers should stop using the product.
Chris A Papas & Son Co is recalling Cherry Easter Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
GE Healthcare is recalling T2100 and T2000 treadmills due to a potential safety issue with the power cord assembly.
Chris A Papas & Son Co is recalling 4,968 Coconut Easter Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
CooperSurgical is recalling MediChoice Infant Heel Warmers because products without expiration dates have a remote potential for minor burns.
Chris A Papas & Son Co is recalling Peanut Butter because the labels fail to declare soy and Yellow #5, which are known allergens.
Twin City Bagel, Inc. is recalling various brands of everything bagels because they may contain undeclared peanuts or almonds.
GE Healthcare is recalling specific ventilator models due to a potential failure of the caster mounting hardware that could cause the device to fall or tip over.
Chris A Papas & Son Co is recalling Pineapple because labels lack required declarations for soy and Yellow #5, known allergens.
Chris A Papas & Son Co is recalling Mint Cream Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Gillig is recalling one Recaro bus driver seat because a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in a crash.
Chris A Papas & Son Co is recalling 4,176 Vanilla Cream Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Ford is recalling 6,322 model year 2011-2015 F-350, F-450, and F-550 trucks equipped with ambulance or fire engine packages due to a software defect that may cause the engine to shut down unexpectedly.
Benson's Old Home Kitchens is recalling Wal-Mart private label Sock It To Me Crème Cakes because they contain undeclared pecans, a major food allergen.
Aron Streit Inc. is recalling Streit's Kids Dark Chocolate Coins because testing revealed undeclared milk, a major allergen.
Rill Foods is recalling Rocky Mountain Chili Spice Soup Seasoning because the cumin used may be contaminated with peanut protein.
Rill Foods is recalling Taneum Canyon Chili mix because the cumin used may be contaminated with peanut protein.
Chris A Papas & Son Co is recalling Milk Chocolate Marshmallow Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Chris A Papas & Son Co is recalling Maple Nut Cream Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Chris A Papas & Son Co is recalling White Opera Cream because the labels fail to declare soy and Yellow #5, which are known allergens.
Chris A Papas & Son Co is recalling Milk Opera Cream because the labels fail to declare soy and Yellow #5, which are known allergens.
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes because some packages may have open seals, potentially compromising sterility.
CooperSurgical is recalling Infant Heel Gel Warmers and The Infant Heel Warmer because products without expiration dates have a remote potential for minor burns.
Chris A Papas & Son Co is recalling Dark Chocolate Marshmallow Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.
Rill Foods is recalling Shoshone Falls Black Bean Soup because the cumin used may be contaminated with peanut protein.
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain catheter kits because open seals may compromise product sterility.
Linon Home Décor is recalling about 3,300 foldable wood patio chairs and bistro sets because they can tip over, causing falls.
Synthes, Inc. is recalling 183 thumb screws for orthopedic aiming arms because incorrect raw material was used, which may lead to stress-corrosion cracking.
GE Healthcare is recalling 472 nuclear medicine systems worldwide because a collimator may fall off during rotation. No injuries have been reported.
Baxter Healthcare is recalling 75 HomeChoice Pro APD systems because the occluder may have sharp edges or separate, causing system errors or therapy termination.
Stryker Howmedica Osteonics is recalling 2,030 Triathlon Distal Capture Assemblies because a weld may disassociate, potentially causing the trigger mechanism to become loose or disassociated.
Smiths Medical is recalling specific lots of 50mL CADD Medication Cassette Reservoirs because they may leak at the sealing area. No serious injuries or deaths have been reported.
Goya Foods is recalling 29-ounce cans of Black Bean Soup and Kirby brand black beans due to possible peanut contamination.
Bard Access Systems is recalling 16,410 units of BD PosiFlush Saline Flush Syringes included in various device kits because open seals may impact product sterility.
Mindray is recalling 519 Passport V Monitors because the invasive blood pressure function may provide incorrect measurements.
Siemens is recalling three ARTISTE MV System linear accelerators due to a software issue that may cause a dark current phenomenon during specific cancer treatments.
CooperSurgical is recalling Fisher Brand Gel and Liquid Infant Heel Warmers because products without expiration dates pose a remote potential for minor burns.
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in various catheter kits because open seals may compromise product sterility.
Transonic Systems Inc is recalling Hemodialysis Monitors that may display zero or low flow values, preventing accurate measurements during dialysis.
Elekta is recalling Precise Treatment Tables because incorrect sensor installation during maintenance can cause undetected positioning errors, potentially leading to clinical mistreatment.
Goya Foods is recalling Kirby Black Beans Creole Seasoning and Goya Black Bean Soup due to possible peanut contamination.
Puritan Medical Products is recalling sterile absorbent foam tipped applicators because the shafts may break, preventing adequate patient specimen collection.
Baxter Healthcare is recalling MiniCap with Povidone-Iodine Solution units for hemodialysis because the product may have separating or protruding sponges.
Mylan Institutional LLC is recalling specific lots of Nicardipine Hydrochloride Injection because the product failed potency and impurity specifications.
Siemens Medical Solutions is recalling 419 Symbia E SPECT systems worldwide because radial motor drives were incorrectly assembled backwards during a customer service action.
Tarmac Products is recalling specific lots of Antacid Liquid Regular Strength because they failed microbiological testing at the 12-month time point.
Siemens Medical Solutions is recalling E.CAM emission computed tomography systems because radial motor drives replaced during service were assembled backwards.
CooperSurgical is recalling NovaPlus infant heel warmers because products without expiration dates may cause minor burns.
Med-logics Inc is recalling 360 units of ML 7090 Calibrated LASIK Blades because they do not fit into the AMO Amadeus Metal Blade Holder.
Radiometer America Inc. is recalling Crea A and B membranes used with ABL800 FLEX analyzers due to negative drift on quality control during their in-use lifetime.
Materialise N.V. is recalling Signature TKA GDE/MDL Set 04-05 surgical guides because images from a different patient were used for production.
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