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. 2,642 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,642 in last 12 months

Showing 261280 of 50,117 recalls

Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing