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. 2,673 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,673 in last 12 months

Showing 2292122940 of 55,896 recalls

Medical DeviceOctober 4, 2019· Neocis Inc.

Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...

The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Randox Laboratories, Limited

Recalled Item: Randox Liquid Cardiac Controls Catalogue Number CQ5051 Recalled by Randox...

The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control model numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Randox Laboratories, Limited

Recalled Item: Randox Liquid Cardiac Controls Catalogue Numbers CQ5053. Recalled by Randox...

The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...

The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Randox Laboratories, Limited

Recalled Item: Randox Liquid Cardiac Controls Catalogue Number CQ5052. Recalled by Randox...

The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Ventana Medical Systems Inc

Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...

The Issue: The firm became aware of a cleaning solution leaking issue from the middle...

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

Class II — Potential Health HazardOngoing
FoodOctober 4, 2019· Gullah Gourmet, Inc.

Recalled Item: Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag Recalled by Gullah...

The Issue: The product ingredient statement does not list walnuts in the product.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2019· Arcadia Trading Inc.

Recalled Item: Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By:...

The Issue: Product contains undeclared sulfites.

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

Class III — Low RiskOngoing
Refund
FoodOctober 3, 2019· G&C Food Distributors, Inc.

Recalled Item: Frozen blackberries Recalled by G&C Food Distributors, Inc. Due to Product...

The Issue: Product is contaminated with norovirus.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Philips North America, LLC

Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...

The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...

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

Class II — Potential Health HazardOngoing