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. 2,653 recalls have been distributed to New Jersey in the last 12 months.
Showing 25621–25640 of 53,621 recalls
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...
The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...
The Issue: The firm has become aware that due to a chemical reaction, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...
The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ultra2 Genesys Variants Analyzer Recalled by Clark Laboratories, Inc....
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys 2 Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys Analytical Column Recalled by Clark Laboratories, Inc. (dba,Trinity...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys Diluent Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys 1 Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...
The Issue: Experienced accelerated battery depletion and a shortened replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.