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. 2,834 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,834 in last 12 months

Showing 59615980 of 29,496 recalls

Medical DeviceJuly 14, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: MobileLink Acetabular Cup System Recalled by Waldemar Link GmbH & Co. KG...

The Issue: Product is labeled with incorrect offset.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· EMPATICA SRL

Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...

The Issue: May have a battery life lasting less than the full 48 hours, requiring the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Instrumentation Laboratory

Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...

The Issue: Sample misidentification could occur under specific conditions and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...

The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...

The Issue: Lipemic interference failed to meet the performance specification listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Olympus Corporation of the Americas

Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...

The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Draeger Medical, Inc.

Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...

The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing