Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Over Deformation Risk
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of the Americas
Devices which
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
4,267 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,267
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Over 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 Sphincterotome Recalled Due to Deformation Risk
Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.
Olympus Corporation of the Americas
Devices which
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Sphincterotome Over 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 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 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
HIGH
FDA DEVICE
Medline Convenience Kits: 1) HYSTEROSCOPY, Model Number: CDS984086I; 2) KIT GYN ONCOLOGY LAP, Model Number: DYKMBNDL91A; 3) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807J; 4) VAGINAL...
Medline Industries, LP
Medline has