Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,111 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,111 in last 12 months

Showing 6981–7000 of 52,570 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· 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 7.1.000 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· 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 7.1.000US 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· 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· 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· 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
DrugJanuary 10, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...

The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2024· BE PHARMACEUTICALS AG

Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...

The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2024· Now Foods

Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...

The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
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· Ventec Life Systems, Inc.

Recalled Item: VOCSN Patient Breathing Package (Pediatric Recalled by Ventec Life Systems,...

The Issue: The bonded spiral wrap may detach before or during ventilation due to a...

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

Class I — Serious Health HazardOngoing