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. 2,638 recalls have been distributed to New York in the last 12 months.
Showing 31961–31980 of 55,896 recalls
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Tibial Trial Handle. To assist the surgeon in the Recalled by...
The Issue: The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringe Bulb Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom HEART CATH TRAY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits Recalled by Avid...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom UPPER EXTREMITY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom GENERAL PACK convenience kits Recalled by Avid Medical, Inc....
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom LAMINECTOMY PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom CATH PACK convenience kits Recalled by Avid Medical, Inc. Due...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.