Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,000 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,000 in last 12 months

Showing 16181–16200 of 48,219 recalls

Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing