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. 2,868 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,868 in last 12 months

Showing 49214940 of 30,153 recalls

Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.1.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.200 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.1.000US Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 9, 2024· Covidien

Recalled Item: Medtronic Invos Recalled by Covidien Due to manufacturing defects to sensor...

The Issue: manufacturing defects to sensor cable connectors may result in error codes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.HASSON TROCAR 10/110MM Recalled by Aesculap Inc Due to The sterile...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing