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. 2,616 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,616 in last 12 months

Showing 46814700 of 28,538 recalls

Medical DeviceFebruary 2, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...

The Issue: Pack and pouch label is missing the manufacturing and expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinets, running affected software, and Windows 10...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Technicality Inc.

Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...

The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing