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. 997 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
997 in last 12 months

Showing 39721–39740 of 53,621 recalls

DrugSeptember 2, 2015· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...

The Issue: Lack of Assurance of Sterility: Recalling firm reported a complaint for mold...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 2, 2015· Sincerely Nuts

Recalled Item: Sincerely Nuts brand Macadamia Nuts (Raw) (a) Whole Recalled by Sincerely...

The Issue: Raw Macadamia Nuts were found to be contaminated with Salmonella based on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 1, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...

The Issue: An issue with a USB memory component contained within a subset of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodAugust 31, 2015· The Ice Cream Club, Inc.

Recalled Item: Caramel Caribou Ice Cream Recalled by The Ice Cream Club, Inc. Due to...

The Issue: Product contains undeclared peanuts

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 31, 2015· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep...

The Issue: Custom Sterile Surgical kits contain 3M DuraPrep (TM) Surgical Solution,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical...

The Issue: Custom Sterile Surgical kits contain 3M DuraPrep (TM) Surgical Solution,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Elekta, Inc.

Recalled Item: XiO Radiation Treatment Planning System. Used to create treatment plans...

The Issue: Incorrect Treatment Delivery Using Third Party Fixed Wedges.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing