Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,566 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,566 in last 12 months

Showing 1156111580 of 28,538 recalls

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 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 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: CMExpress Microbore Set 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 Set 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 Needleless Adaptor 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: 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: CMExpress Microbore Set 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: 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 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 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
Medical DeviceJune 15, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...

The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...

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

Class II — Potential Health HazardOngoing