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. 2,632 recalls have been distributed to New Jersey in the last 12 months.
Showing 33701–33720 of 53,621 recalls
Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Phosphate and Benzoyl Peroxide Gel Recalled by L. Perrigo...
The Issue: Microbial Contamination of Non-Sterile Product; small number of tubes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Superpotent...
The Issue: Superpotent Drug; out of specification results for assay (manufacturer)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...
The Issue: The affected products have approximately a 91% specificity while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...
The Issue: May experience a loss of centralized monitoring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Foods Markets Lobster Bisque Distributed by: Whole Foods Market...
The Issue: Back label of Lobster Bisque product was mislabeled as Butternut Squash Soup...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES Recalled by Roland Foods,...
The Issue: Product quality issue. Through sampling, FDA revealed the presence of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X upgraded to XCT 882454 Recalled by Philips Medical Systems...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.