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. 2,598 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,598 in last 12 months

Showing 79417960 of 28,538 recalls

Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Hemoglobin A1c for use with Architect Recalled by Abbott Laboratories Due to...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve ZELTIQ Vaccum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve+ ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCore ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott

Recalled Item: Abbott TactiCath Sensor Enabled Recalled by Abbott Due to When connected to...

The Issue: When connected to the EnSite Precision Navigation System, an affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome HSI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision Chronic Catheter Recalled by Covidien Llc Due to There...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision HSI Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome H Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome SI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Mahurkar Chronic Carbothane (Maxid) Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision H Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision SI Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2022· Covidien Llc

Recalled Item: TruClear Hysteroscopic Tissue Removal System Control Unit- designed to meet...

The Issue: Electrical component failure within the control unit. The observed failure...

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

Class II — Potential Health HazardOngoing