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. 2,879 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,879 in last 12 months

Showing 321340 of 53,621 recalls

DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: BioGlo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: Bio Glo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: Vista Tears Polyethylene Glycol 400 0.4% w/v Recalled by Wizcure Pharmaa...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: Vista Gel Hypromellose USP 0.3% w/v Recalled by Wizcure Pharmaa Private...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: Vista Gonio Eye Lubricant Recalled by Wizcure Pharmaa Private Limited Due to...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Recalled by...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Wizcure Pharmaa Private Limited

Recalled Item: CHNaO Fluorescein Sodium Ophthalmic Strips Recalled by Wizcure Pharmaa...

The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· Alvogen, Inc

Recalled Item: Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Product Mix-Up:...

The Issue: Product Mix-Up: A single bottle of this lot was reported by a pharmacy to...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 31, 2025· AvKARE

Recalled Item: Rosuvastatin Tablets Recalled by AvKARE Due to Out of specification for...

The Issue: Out of specification for dissolution.

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

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

Recalled Item: Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET...

The Issue: Under circumstances involving exposure to particular chemicals and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2025· Centinel Spine, Inc.

Recalled Item: Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number:...

The Issue: Products were mislabeled as the 6mm product but included the 5 mm product.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2025· Miach Orthopaedics

Recalled Item: BEAR Implant. Model Number: 1000. Recalled by Miach Orthopaedics Due to...

The Issue: Incorrect expiration date on label that extends beyond the product's...

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

Class II — Potential Health HazardOngoing
DrugDecember 30, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Icosapent Ethyl capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Subpotent Drug: Due oxidation caused by leakage of the contents of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Fluocinolone Acetonide Solution Topical Solution USP Recalled by SUN...

The Issue: Failed Impurities/Degradation Specifications: Out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugDecember 30, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ondansetron Orally Disintegrating Tablets Recalled by Glenmark...

The Issue: Defective container: Preferred Pharmaceuticals received a letter from the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2025· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 Surgeon Console Viewer Display Recalled by Intuitive Surgical,...

The Issue: Robotic-assisted surgical system has Viewer Display manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R Recalled by...

The Issue: Ortho images acquired with preset automatic horizontal flip are not flipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2025· Cerapedics, Inc.

Recalled Item: PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft Recalled by...

The Issue: Incorrect expiration date

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T Recalled by...

The Issue: Ortho images acquired with preset automatic horizontal flip are not flipped...

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

Class II — Potential Health HazardOngoing
DrugDecember 26, 2025· Haleon US Holdings LLC

Recalled Item: parodontax (cetylpyridinium chloride)ACTIVE GUM HEALTH Recalled by Haleon US...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or...

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

Class III — Low RiskOngoing
Refund