Recalls affecting New Jersey
Notices that name New Jersey in their distribution area, plus every nationwide recall — nationwide recalls reach New Jersey too.
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Class III · 7 months ago
Winder Laboratories, LLC Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recall: Subpotent. During an FDA inspection it was discovered that the product
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
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Class II · 7 months ago
Wawa Reduced Fat Milk 2% 16 oz recall: Foreign plastic material discovered on fill line
Foreign plastic material discovered on fill line.
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Class I · 7 months ago
Amneal Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag recall: A Magnesium Sulfate in Water for Injection pouch was found to contain an IV
A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride Injection, 10 mg/mL.
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NHTSA safety recall · 7 months ago
Toyota recall: The load carrying capacity modification label may display inaccurate added
The load carrying capacity modification label may display inaccurate added weight values. As such, these vehicles fail to comply with the…
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Public Health Alert · 7 months ago
White Oak Pastures Public Health Alert for Ground Beef products recall: Product Contamination
Product Contamination
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Elevated risk · 8 months ago
Gold Lion, ilum Chocolate recall: Product contains sildenafil and tadalafil
Product contains sildenafil and tadalafil
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NHTSA safety recall · 8 months ago
Ford recall: The Image Processing Module A (IPMA) may experience multiple unexpected
The Image Processing Module A (IPMA) may experience multiple unexpected resets, resulting in loss of the rearview camera image and advanced driver…
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Highest risk · 8 months ago
Tainoki Fine Furniture Office Chairs recall: Risk of Serious Injury and Fall Hazard
Risk of Serious Injury and Fall Hazard
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Highest risk · 8 months ago
Lifetime Brands Built Luum Light Up Tumblers recall: Risk of Choking and Battery Ingestion Hazards
Risk of Choking and Battery Ingestion Hazards
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Highest risk · 8 months ago
Electrolux Group Frigidaire Gas Ranges recall: Burn Hazard
Burn Hazard
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
Boston Scientific Corporation EndoVive Safety PEG Kit recall: Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result…
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Class II · 8 months ago
Altruan GmbH Wondfo Streptococcal A At-Home Self-Test. At-home test for group recall: Product not cleared by the FDA
Product not cleared by the FDA.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class III · 8 months ago
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class II · 8 months ago
Altruan GmbH Brand Name: Bisaf Strep A Self-Test. Test for detection of group recall: Product not cleared by the FDA
Product not cleared by the FDA.
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Class II · 8 months ago
Medartis AG Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7 recall: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model SL Connection Component incl. PE-Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…