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. 2,834 recalls have been distributed to New Jersey in the last 12 months.
Showing 6181–6200 of 53,621 recalls
Recalled Item: Grande Lactose SKU 30600. Grade A. Pasteurized. Net Wt Recalled by GRANDE...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Grande Primo Y45 Cultured Dairy Product. Product Code: 32400....
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Protein. Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Bravo 500 Functional Whey Protein SKU 32103. 34% Protein. Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sirolimus Tablets 1mg Tablets 100-count bottle Recalled by Dr. Reddy's...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...
The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 8mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 4mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection Recalled...
The Issue: Labeling: Wrong Barcode
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...
The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...
The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...
The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BSM-3000 Series Bedside Monitor The Life Scope BSM-3000 Recalled by Nihon...
The Issue: Due to software issue the device may give false "SpO2 Probe Failure" alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.