Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,722 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,722 in last 12 months

Showing 48614880 of 29,286 recalls

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 7.1.000US 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· 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· 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 7.2.000 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· 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· 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 7.1.000 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 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...

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.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...

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
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W. DILATING PIN 10/110MM Recalled by Aesculap Inc Due to The...

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
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· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" 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