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. 2,636 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,636 in last 12 months

Showing 16411660 of 28,538 recalls

Medical DeviceMay 8, 2025· CareFusion 303, Inc.

Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...

The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2025· Ohio Medical Corporation

Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...

The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2025· BALT USA, LLC

Recalled Item: Prestige Coil System /UDI-DI codes: PRES0153CXPPLT 00810068567311...

The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2025· BALT USA, LLC

Recalled Item: Optima Coil System /UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK...

The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2025· LUMITHERA INC

Recalled Item: Brand Name: Valeda Light Delivery System Product Name: Light Based Recalled...

The Issue: U.S. customers were shipped devices that were configured for the European...

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

Class III — Low RiskOngoing
Medical DeviceMay 7, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer C11137 Recalled by Beckman Coulter,...

The Issue: Analyzer has calibration issues where curves switched from passed to failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2025· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name:...

The Issue: Electrode placement labels on the Digital Acquisition Box (DAB) were applied...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2025· Zyno Medical LLC

Recalled Item: Z-800 Infusion System. Intended to provide intravenous infusion of...

The Issue: Unreleased software versions were installed on distributed devices without...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2025· MicroAire Surgical Instruments, LLC

Recalled Item: Brand Name: SmartRelease ESTR (Endoscopic soft tissue release system)...

The Issue: Potential that the blade can unintentionally cut tissue prior to the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2025· Zyno Medical LLC

Recalled Item: Z-800WF Infusion System. Intended to provide intravenous infusion of...

The Issue: Unreleased software versions were installed on distributed devices without...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2025· Zyno Medical LLC

Recalled Item: Z-800W Infusion System. Intended to provide intravenous infusion of...

The Issue: Unreleased software versions were installed on distributed devices without...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2025· Zyno Medical LLC

Recalled Item: Z-800F Infusion System. Intended to provide intravenous infusion of...

The Issue: Unreleased software versions were installed on distributed devices without...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive...

The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium...

The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable...

The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...

The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Baxter Healthcare Corporation

Recalled Item: Affinity 4 Birthing Bed Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for improper crimps on the signal wires of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2025· Copan WASP

Recalled Item: PhenoMATRIX Recalled by Copan WASP Due to AI-powered bacterial culture plate...

The Issue: AI-powered bacterial culture plate interpretation and workup software does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V Recalled...

The Issue: Recent post-market surveillance data suggests a possible association of...

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

Class II — Potential Health HazardOngoing