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. 2,573 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,573 in last 12 months

Showing 1108111100 of 28,538 recalls

Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc....

The Issue: Product not properly being aligned with the adequate gamma sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055 Recalled by...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet Regenerex Primary Taper Cap Item Number 141269 Recalled by Biomet,...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· AB ULAX

Recalled Item: 1500 Flex Heat and Moisture Exchanger Recalled by AB ULAX Due to Firm has...

The Issue: Firm has received 6 complaints that the Heat Moisture Exchanger (HME)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2020· Biomet, Inc.

Recalled Item: Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050 Recalled by Biomet,...

The Issue: Product not properly being aligned with the adequate gamma sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2020· Biomet, Inc.

Recalled Item: (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar...

The Issue: Zimmer Biomet is conducting a medical device recall for three lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2020· Biomet, Inc.

Recalled Item: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper...

The Issue: Product potentially being packaged without a taper adapter or baseplate. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2020· Gentian AS

Recalled Item: GENTIAN Cystatin C Calibrator and Calibrator Kit Recalled by Gentian AS Due...

The Issue: The firm has identified lots of calibrators that have shown to measure...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Appx 1.7 ml Bag Spike w/Integrated Clave Recalled by ICU Medical, Inc. Due...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 76 cm (30") Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 31" (78 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing