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. 2,874 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,874 in last 12 months

Showing 12211240 of 29,496 recalls

Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....

The Issue: Potential that a component (air baffle) may be missing in some Nehalem...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee System Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Lumicell, Inc.

Recalled Item: Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product...

The Issue: The potential of the elastic bands included in the kit detaching or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· S.I.N. Implant System Ltda

Recalled Item: IMPLANT EPIKUT PLUS MT16 3 Recalled by S.I.N. Implant System Ltda Due to...

The Issue: Dental implants were imported under temperature and storage conditions that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· Contract Medical International GmbH

Recalled Item: Brand Name: Fortress Introducer Sheath System Product Name: Fortress...

The Issue: Units may have been packaged with an incorrect pouch label, which lists the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Clearview Strep A Exact II Dipstick Respiratory Kit Recalled by Mckesson...

The Issue: Due to a classification error in the inventory management system, specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales...

The Issue: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600...

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

Class II — Potential Health HazardOngoing