State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wegmans is recalling Apple Cranberry Crostata products because they contain undeclared soy lecithin. The products were sold in New York, New Jersey, Massachusetts, Virginia, and Maryland.
Wegmans Food Markets is recalling Nectarine Crostata products due to undeclared soy lecithin, a potential allergen hazard.
Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.
Penobscot McCrum LLC is recalling Medium Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.
Fairway Group Holdings Corp is recalling 323 units of Cookies Blondie due to undeclared walnuts. The product was distributed in New York, New Jersey, and Connecticut.
Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Penobscot McCrum LLC is recalling 951 cases of Medium Coated Jo-Jo Wedges because the product may contain undeclared milk.
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Penobscot McCrum LLC is recalling 18,799 cases of seasoned baby Jo-Jo wedges because the product may contain undeclared milk.
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.
Wegmans is recalling Apple Crostata products due to undeclared soy lecithin, a potential allergen hazard for sensitive consumers.
Wegmans Food Markets is recalling Peach Crostata products due to undeclared soy lecithin. The products were sold in New York, New Jersey, Massachusetts, Virginia, and Maryland.
Penobscot McCrum LLC is recalling Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
Medtronic is recalling eight AxiEM ENT suction kits because the instruments fail mandatory pre-use verification tests.
Medtronic is recalling 15 Fusion ENT Instrument Kits because the instruments fail pre-use verification. The kits were distributed in the US and Canada.
Penobscot McCrum LLC is recalling 5,782 cases of Medium Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.
Penobscot McCrum LLC is recalling 21,560 cases of Broaster Recipe Crinkle Cut Seasoned Wedges because the product may contain undeclared milk.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 60 mg, due to a label mixup that may result in mislabeling.
C. O. Truxton is recalling Phenobarbital Tablets USP, 100 mg, due to a label mixup that may result in mislabeled products.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 500 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 13 reusable ENT instrument sets because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.