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 521540 of 53,621 recalls

DrugDecember 12, 2025· Medinatura New Mexico, inc.

Recalled Item: ClearLife Allergy Nasal Spray Recalled by Medinatura New Mexico, inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: The products have been...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Bard Peripheral Vascular Inc

Recalled Item: Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Recalled...

The Issue: Due to damage to outer tray that can potentially compromise the sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Hologic, Inc

Recalled Item: ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. Recalled by...

The Issue: Fungal contamination of affected lot with Parengyodontium album.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the Recalled...

The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Philips North America Llc

Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...

The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Recalled...

The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number:...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing