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. 2,873 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,873 in last 12 months

Showing 37213740 of 55,896 recalls

Medical DeviceJanuary 3, 2025· LivaNova USA, Inc.

Recalled Item: Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva" Recalled by...

The Issue: Their is a potential that implanted pulse generators may stop delivering...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2025· LivaNova USA, Inc.

Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...

The Issue: Their is a potential that implanted pulse generators may stop delivering...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Scientia Vascular, Inc.

Recalled Item: Socrates 38 Aspiration Catheter 127 cm length The Recalled by Scientia...

The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· US Endodontics, LLC

Recalled Item: Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK...

The Issue: Due to devices being irradiated above the established specification which my...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Beckman Coulter Inc.

Recalled Item: Access PCT Reagent Pack Recalled by Beckman Coulter Inc. Due to Identified...

The Issue: Identified reagent lots are experiencing a high rate of calibration failures...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Belmont Instrument LLC

Recalled Item: Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Recalled...

The Issue: Disposable set may leak during priming from a female quick connector due to...

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

Class II — Potential Health HazardOngoing
FoodDecember 31, 2024· The Granola Bar

Recalled Item: The Granola Bar brand The OG Bar Recalled by The Granola Bar Due to...

The Issue: Product contains undeclared milk and soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 31, 2024· Exactech, Inc.

Recalled Item: AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL Recalled...

The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2024· Exactech, Inc.

Recalled Item: Novation XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled...

The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2024· Exactech, Inc.

Recalled Item: Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled by...

The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...

The Issue: The catheter subassembly in the Integrated Arterial Catheter was...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 31, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT Recalled...

The Issue: The catheter subassembly in the Integrated Arterial Catheter was...

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

Class I — Serious Health HazardOngoing
FoodDecember 30, 2024· V Chocolates, Inc

Recalled Item: Assorted Chocolate Caramels with kosher sea salt Recalled by V Chocolates,...

The Issue: Small pieces of plastic broken tray in the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 30 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine DR Capsules USP 60 mg Recalled by Rising Pharma Holding, Inc. Due...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 20 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2024· Neilmed Pharmaceuticals Inc

Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...

The Issue: Due to nasal spray stability failure for bioburden.

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2024· Eugia US LLC

Recalled Item: Progesterone Injection USP Recalled by Eugia US LLC Due to Presence of...

The Issue: Presence of Particulate Matter: A market complaint was received of a glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Prograf (tacrolimus) capsules Recalled by Astellas Pharma US Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Astagraf XL (tacrolimus extended-release capsules) 0.5 mg Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund