Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,901 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,901 in last 12 months

Showing 761780 of 55,896 recalls

FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC MORINGA LEAF POWDER Recalled by Lexunder Inc Due...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2025· Lexunder Inc

Recalled Item: Food to Live brand ORGANIC SUPERGREENS POWDER MIX Recalled by Lexunder Inc...

The Issue: Contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 11, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Varenicline Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Sub...

The Issue: Sub potent drug: during the 9-month stability test conducted, the assay...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· Medline Industries, LP

Recalled Item: DEXLOCK Achilles Repair Implant Kits Recalled by Medline Industries, LP Due...

The Issue: There have been multiple complaints of drill bit fusing to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2025· Beckman Coulter, Inc.

Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...

The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 60 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 45 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 55 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
FoodNovember 8, 2025· ByHeart, INC.

Recalled Item: 1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams Recalled by...

The Issue: Contaminated with Clostridium botulinum

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 7, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Da Vinci Product Name: da Vinci X Recalled by Intuitive...

The Issue: Due to a software implementation error that allowed instruments arms failing...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 19927 Kirkland Signature Caesar Salad Recalled by Costco...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Carton label: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Defective Container - A defect in the side-seal which allows leakage of product.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 7, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...

The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...

The Issue: Due to a number of modules flashed with a date and time associated with the...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2025· Fresenius Kabi USA, LLC

Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

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

Class I — Serious Health HazardOngoing
Refund