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 35413560 of 30,153 recalls

Medical DeviceJuly 24, 2024· TMJ Solutions Inc

Recalled Item: Stryker TMJ Unilateral Implant Recalled by TMJ Solutions Inc Due to...

The Issue: Patient-fitted temporomandibular (TMJ) prothesis contained incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cardinal Health 200, LLC

Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube Recalled by Cardinal...

The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· ROi CPS LLC

Recalled Item: regard Clinical Packaging Solutions Recalled by ROi CPS LLC Due to Medical...

The Issue: Medical convenience kits were distributed with Merit syringes (manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Sensors Recalled by Abbott Diabetes Care, Inc. Due to...

The Issue: Users of the FreeStyle Libre 3 sensors reported situations where they were...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 2.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 5.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cypress Medical Products LLC

Recalled Item: McKesson Syringe 60CC Recalled by Cypress Medical Products LLC Due to...

The Issue: Affected syringes lack FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Match Head Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Match Head Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing