Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,110 recalls have been distributed to New Jersey in the last 12 months.
Showing 13981–14000 of 53,621 recalls
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...
The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...
The Issue: The QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...
The Issue: Misprinted expiration date on the shelf-box
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...
The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...
The Issue: Software issue for treatment plan and image management application may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...
The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Natural Dentist Healthy Breath Antiseptic Rinse Recalled by Revive...
The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...
The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: quinapril HCl/hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...
The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...
The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.