State
73,817 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Hazelnut bars due to undeclared peanut. Consumers should stop eating these bars.
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.
Chicago Bar Company LLC is voluntarily recalling RXBAR Mango Pineapple bars because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling Chocolate Sea Salt RXBARs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Maple Sea Salt bars due to an undeclared peanut allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Blueberry bars due to the presence of undeclared peanut, a major food allergen.
Avella of Deer Valley, Inc. is recalling 2,840 syringes of Labetalol 20mg Injectable Solution because the 2D barcodes contain incorrect expiration dates.
Avella of Deer Valley is recalling 4,950 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Philips is issuing a software update for 24 Ingenuity TF PET/CT systems to correct multiple issues identified in the previous software version.
Ottobock is recalling 538 PushValve units because some valve inserts have a diameter smaller than the specification. The valve is used for prosthetic fitting of lower limb amputees.
Valeant Pharmaceuticals is recalling 390 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Signature Orthopedics is recalling 10 Genius Knee Cemented Tibial Components due to a product mix-up. The recall covers units distributed in Florida, New York, and Tennessee.
US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.
Valeant Pharmaceuticals is recalling 22 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Ottobock is recalling 110 MagValve units used in prosthetic sockets because some valve inserts have a smaller diameter than specified.
Valeant Pharmaceuticals is recalling 206 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, meaning the drug may not release properly.
Avella of Deer Valley is recalling 8,500 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Ottobock is recalling PushValve upper parts because some installed valve inserts have a diameter smaller than the specification.
Avella of Deer Valley is recalling 250 bags of compounded magnesium sulfate due to incorrect expiration dates in the 2D barcodes.
Valeant Pharmaceuticals is recalling 1,023 bottles of Cardizem CD (diltiazem hydrochloride) 120 mg capsules because they failed to meet dissolution specifications.
Valeant Pharmaceuticals is recalling 23,884 bottles of Diltiazem HCl CD capsules because they failed dissolution specifications, potentially affecting drug release.
Dr. Reddy's Laboratories is recalling Esomeprazole Magnesium 40mg capsules because they may contain brown pellets.