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. 2,658 recalls have been distributed to New Jersey in the last 12 months.
Showing 23681–23700 of 29,496 recalls
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSCalibur Recalled by BD Biosciences, Systems & Reagents Due to The...
The Issue: The circuit breakers on some BD FACSCalibur instruments may have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YC-1800 OPHTHALMIC YAG LASER SYSTEM Recalled by Nidek Inc Due to Dear Doctor...
The Issue: Dear Doctor letter and Quick Guide is being sent to users of the YC-1800 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...
The Issue: Needle is leaking from hub/needle cannula connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...
The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...
The Issue: There is a potential for duplicate container numbers to be created for patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamondback 360 Coronary Orbital Atherectomy System Recalled by...
The Issue: The OAD saline sheath outer layer may flake off from the catheter due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...
The Issue: The threads of the outer tube of the shock module of LP Rotate are too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.