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 51415160 of 28,538 recalls

Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Keystone Industries

Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...

The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit N10 Nasal Masks and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...

The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 - IVD For use as a Recalled by Randox Laboratories...

The Issue: Target for Alkaline Phosphatase (ALP) for the AMP optimized to IFCC 37¿C...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...

The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2023· Philips North America Llc

Recalled Item: Panorama 1.0T HFO Recalled by Philips North America Llc Due to Firm was...

The Issue: Firm was informed of an event in which the structural integrity of the MR...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 16, 2023· Becton Dickinson & Company

Recalled Item: PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL...

The Issue: An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2023· Covidien

Recalled Item: Covidien Valleylab FT10 Recalled by Covidien Due to Due to software issue,...

The Issue: Due to software issue, New systems may exhibit an error which may prohibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2023· Steris Corporation

Recalled Item: V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty...

The Issue: Bandage Scissors handle cover component contains an incorrect color...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2023· Covidien LP

Recalled Item: AbsorbaTack Absorbable Fixation Device 30 Violet Absorbable Tacks 5 mm-...

The Issue: Packaging of the device may cause a low seal strength in the side seal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· SoClean, Inc

Recalled Item: SoClean 3 Recalled by SoClean, Inc Due to New User Manual with additional...

The Issue: New User Manual with additional instructions for use and a hose and mask...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE TRAY TRACH BASIC SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· Medtronic MiniMed, Inc.

Recalled Item: Guardian 4 Glucose Sensor Recalled by Medtronic MiniMed, Inc. Due to Some...

The Issue: Some sensors may have a glucose oxidase (GOX) layer thickness outside of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· Spectranetics Corporation

Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX Spectranetics...

The Issue: Incorrect product labeling. Exterior product box label does not match...

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

Class II — Potential Health HazardOngoing