Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,863 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,863 in last 12 months

Showing 161180 of 29,505 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
Medical DeviceJanuary 6, 2026· Straumann USA LLC

Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...

The Issue: The mix up of the impression caps provided in the package. The provided...

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

Class III — Low RiskOngoing