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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 27721–27740 of 29,496 recalls
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...
The Issue: Out of specification result - stability test failure of free available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...
The Issue: Philips was notified of a problem using the IntelliSpace Portal with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...
The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD ProbeTec Neisseria gonorrhoeae (GC) Qx Amplified DNA Assay Reagent Pack...
The Issue: Increased levels of false positives in BD Probe Tech Neisseria gonorrhoeae Q...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...
The Issue: Possibility that the inner pouch may be compromised. The product is packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) Recalled...
The Issue: GE Healthcare has become aware of a potential safety issue due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERNAL HEX RECON SCREW Recalled by Smith & Nephew Inc Due to 75 mm screws...
The Issue: 75 mm screws were packaged and labeled using an 80 mm screw outer box and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were...
The Issue: The cassettes were shipped with the wrong IP (image plate) size bar code.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...
The Issue: Increased risk of failure at the driver tip during screw insertion or removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERNAL HEX RECON SCREW Recalled by Smith & Nephew Inc Due to 75 mm screws...
The Issue: 75 mm screws were packaged and labeled using an 80 mm screw outer box and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heritage Labs Path Study Extra Supplies Kit Recalled by Heritage Labs...
The Issue: The product has a Lithium Heparin contaminant which could adversely affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.