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. 1,053 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,053 in last 12 months

Showing 11341–11360 of 27,462 recalls

Medical DeviceJune 17, 2020· Resource Optimization & Innovation LLC

Recalled Item: regard Migrating Indicator Recalled by Resource Optimization & Innovation...

The Issue: The firm received reports from customer that the Regard Migrating Indicator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: CMExpress Needleless Y Site Microbore Set Recalled by CME America, LLC Due...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset With Female Luer Recalled by CME America, LLC Due to...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard BodySet Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard set with Female Luer Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset with Filter Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset with Filter and Manual Priming Valve Recalled by CME...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: Standard BodySet with Needleless Connectors Recalled by CME America, LLC Due...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset with Male Luer Connectors Recalled by CME America, LLC...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset w/ Non-Vented Spike Connector Recalled by CME America,...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing