Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Performance Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome V Due to Deformation Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Sphincterotome Recalled Due to Performance Risks
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Risk of Deformation
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Single Use 3-Lumen Sphincterotome Due to Performance Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Performance Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Hazardous Deformation Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Potential Deformity Hazard
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Performance Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Performance Risks
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Over Risk of Deformation
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Sphincterotome Recalled Due to Deformation Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to High Risk of Deformation
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Over Potential Performance Issues
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to High Hazard Risk
Olympus Corporation recalled 887 units of the Disposable Triple Lumen Sphincterotome on January 7, 2026. The devices may deform and lose performance if not properly thermoformed. The recall affects both US and international markets.
Olympus Corporation of the Americas
Devices which
Food & Beverages
HIGH
FDA FOOD
Hannaford Dill Pickle Chips Recalled Due to Glass Contamination
Hannaford Bros. Co. recalled 2,484 cases of hamburger dill pickle chips due to glass contamination. Consumers reported finding glass in the product. The recall affects jars sold in Maine and New York.
Mount Olive Pickle Company
Glass in
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Deformation Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Risk of Deformation
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Due to Performance Risks
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Single Use Sphincterotome Over Performance Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
Tag Statistics
Total Recalls
2,756