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. 2,766 recalls have been distributed to New Jersey in the last 12 months.
Showing 14861–14880 of 29,496 recalls
Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...
The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...
The Issue: The product contains a misprinted expiration date on the peel pack. Both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...
The Issue: The polarity of the output of power supply was reversed. Due to polarity of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kendall SCD Express Sterile Sleeves (Thigh Length) Recalled by COVIDIEN LLC...
The Issue: The product does not meet sterility requirements. Product labeled as sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...
The Issue: Potential for the sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...
The Issue: Complaints received that products packaged with the incorrect introducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...
The Issue: The firm became aware of the potential for the products' sterile pouch to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.