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. 2,851 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,851 in last 12 months

Showing 68416860 of 30,153 recalls

Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800753005 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 880393003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 11mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880353009 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880473001 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 12mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 8 mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Becton Dickinson & Co.

Recalled Item: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software Recalled by...

The Issue: Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System with software versions: R2.2.O Recalled by PHILIPS...

The Issue: Potential Loss of X-ray-When the full disk capacity is reached, X-Ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Aesculap Implant Systems LLC

Recalled Item: Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and...

The Issue: Potential for the spring to become loose and fall out of the device, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2023· Linkbio Corp.

Recalled Item: LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP Recalled by Linkbio...

The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...

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

Class II — Potential Health HazardOngoing