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. 1,059 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,059 in last 12 months

Showing 16001–16020 of 50,117 recalls

Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033 Recalled by Cardinal...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: VAPORIZER VICKS 1.5GAL Item Number: 2354942 Recalled by Cardinal Health Inc....

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: DEXCOM G6 SENSOR 3 PACK Item Number: 5447552 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877 Recalled...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Biomerieux Inc

Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...

The Issue: bioMerieux received complaints about calibration issue observed on several...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· B. Braun Medical, Inc.

Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....

The Issue: BBMI has identified through complaints the potential for the extension set...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· Medline Industries Inc

Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...

The Issue: Possible false negative or false positive results due to the product being...

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

Class II — Potential Health HazardOngoing