State
73,106 recalls have nationwide distribution and so reach New Jersey. 9,767 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,767 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,486 (25%) are Severe.
Which agencies issued them
These figures cover only the 9,767 recalls whose distribution notice names New Jersey specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Danisco USA Inc. is recalling Grindsted Creamer 1817 Stabilizer System due to potential Salmonella contamination. The product was distributed to 23 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Reese SG FR Sweetener Blend, CM50 due to potential Salmonella contamination. The recall affects product distributed across 24 US states, Canada, and Mexico.
Danisco USA Inc. recalls CRE-90 (RO1) 25 KG bags due to potential Salmonella contamination. The product was distributed across 24 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted GSD 1076 Stabilizer and Emulsifier System in 50-pound bags due to potential Salmonella contamination. The product was distributed to multiple US states, Canada, and Mexico.
Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted CFF 1455 Stabilizer System due to potential Salmonella contamination. The product was distributed to commercial customers in 24 US states, Canada, and Mexico.
Danisco USA Inc. recalls ASC 2138 Stabilizer and Emulsifier System due to potential Salmonella contamination. Affected product distributed across US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across 28 U.S. states, Canada, and Mexico.
Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.
Schreiber Foods Inc is recalling 835,721 units of Essential Everyday Blueberry Cream Cheese Spread (8 oz) due to potential Salmonella contamination. No illnesses have been reported.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider mechanism from the core component, which could compromise device integrity.
Atrium Medical Corporation recalled 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Patients should consult their healthcare provider regarding appropriate follow-up care.
Schreiber Foods Inc is recalling Strawberry Cream Cheese Spread sold under brands including Fareway, Happy Farms, Hy-Vee, and Schnuck due to potential Salmonella contamination. Approximately 835,721 units were distributed across multiple states and Puerto Rico.
CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.
Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.
Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.
Medline is recalling 25.2 million Luer Lock disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity. The inaccuracy may pose a risk to patient health.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. No injuries have been reported.
Atrium Medical Corporation recalls FLIXENE vascular graft devices due to reported separation of the Slider GDS Swivel Rod from its core, which could affect device function.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to complaints of separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units have been distributed worldwide.
Atrium Medical Corporation is recalling the ADVANTA VXT vascular graft due to reported separation of the Swivel Rod from the Swivel Core. The component separation poses a risk of device failure.