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. 2,683 recalls have been distributed to New Jersey in the last 12 months.
Showing 22161–22180 of 29,496 recalls
Recalled Item: Gold-Tite Hexed Retaining Screw 3mm Item: GSH30 Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Twist Lock TM Straight Transfer Coping Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Ring Abutment 4.1mm(D) x 6mm(H) Item: OSO60 Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Implant Cover Screw Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical Healing Cap Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provide Impression Coping Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain EP Healing Abutment 5mm(D) x 5.6mm(P) x 4mm(H) Item: Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Stop Dental implants Recalled by Biomet 3i, LLC Due to Pouches may not...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Abeon Medical...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona EM Distal Rod Recalled by Zimmer, Inc. Due to Complaints that the...
The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...
The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona EM Proximal Tube Recalled by Zimmer, Inc. Due to Complaints that the...
The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)...
The Issue: Mitek identified that on VAPR Tripolar 90 Degree Suction Electrode the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.