State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
RH is recalling Callum Canopy Beds because horizontal canopy rails can detach and fall. No injuries have been reported, but consumers should stop using the beds until repaired.
Mobility Transportation Services is recalling modified Ford and Ram vans because foldaway seats may not stay locked during a crash, increasing injury risk.
USA LESS Inc. is recalling Leopard Miracle Honey because it contains undeclared sildenafil, an unapproved drug for erectile dysfunction.
Theo Chocolate is recalling Sea Salt 70% Dark Chocolate bars due to undeclared milk. The product was distributed nationwide.
Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA testing found an impurity above acceptable levels.
Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.
Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.
McDaniel Life-Line LLC is voluntarily recalling 150 vials of Indian Herb Paste because the product is an unapproved new drug. The recall covers distribution in the US, Italy, Australia, Canada, and Poland.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 25 mg, because FDA labs found an impurity above acceptable levels.
Hyundai is recalling 12,438 2019 Veloster vehicles because the driver's door latch can fail in a side impact crash, potentially allowing the door to open.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 100 mg, because FDA testing found an impurity above acceptable levels.
Newly Weds Foods Inc is recalling 24,950 lbs of Commercial Breader Batter because it may contain small pieces of plastic.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found an impurity above acceptable levels.
BMW is recalling 2018 i3 electric and hybrid vehicles because a circuit board defect may cause a loss of propulsion, increasing crash risk.
Heat Hero LLC is recalling about 20,000 portable mini heaters because they can overheat, smoke, and catch fire, posing fire and burn hazards.
Spartan Motors is recalling 2019 Utilimaster Truck Bodies because undersized wires may overheat, melt, and cause an unexpected engine shutdown, increasing crash risk.
Volvo is recalling 2016 XC90 vehicles because a coolant hose may crack and leak, potentially causing a fire in the catalytic converter area.
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to a reported leak between the cardioplegia and pressure lumens.
Good Karma Foods is recalling Trader Joe's Natural Creamer - Vanilla because the product contains milk but the label does not list it as an ingredient.
DePuy Orthopaedics is recalling CORAIL AMT COXA VARA Neck Segments because debris or material may be found behind the O-rings.
Abbott Laboratories is recalling 1,666 ARCHITECT c16000 Processing Modules worldwide because unresolved error codes may cause the instrument to generate incorrect diagnostic results.
Glenmark Pharmaceuticals is recalling 2,076 bottles of Pravastatin Sodium 20 mg tablets because a foreign tablet was found in the product.
Becton Dickinson is recalling 6.5 million blood collection assemblies because the luer could break, causing leaks or blocking dialysis ports.
DePuy Orthopaedics is recalling CORAIL AMT High Offset Neck Segments because debris or material may be found behind the O-rings.
Siemens is recalling syngo.CT Cardiac Function software due to a potential risk of wrong measurement in the annulus plane during TAVI planning.