Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,564 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,564 in last 12 months

Showing 261280 of 47,970 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 (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
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: Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable...

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 Sphincterotome V (Distal Wire guided) Model/Catalog...

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: 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
FoodJanuary 6, 2026· Herbs Forever

Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen

The Issue: Potential undeclared allergen ingredient (Wheat)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund