electrical hazard Recalls

Olympus Recalls Sphincterotome Due to Performance Risk

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

Olympus Recalls Sphincterotome Due to Hazardous Deformation Risk

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

Olympus Recalls Sphincterotome Due to Performance Risk

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

Olympus Recalls Sphincterotome Due to Performance Risks

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

Olympus Recalls Sphincterotome Over Risk of Deformation

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

Olympus Sphincterotome Recalled Due to Deformation Risk

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

Olympus Recalls Sphincterotome Due to High Risk of Deformation

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

Olympus Recalls Sphincterotome Over Potential Performance Issues

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

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 Recalls Sphincterotome Due to Deformation Risk

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

Olympus Recalls Sphincterotome Due to Risk of Deformation

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

Olympus Recalls Sphincterotome Due to Performance Risks

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

Olympus Recalls Single Use Sphincterotome Over Performance Risk

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

Olympus Recalls Sphincterotome Over Deformation Risk

Olympus Corporation of the Americas recalled 17,655 sphincterotomes on January 7, 2026. The devices may deform due to improper thermoforming, affecting performance. Patients and healthcare providers must stop using the devices immediately.

Olympus Recalls Sphincterotome Due to Deformation Risk

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

Philips North America Recalls CT Scanner Over Rotor Fastener Issue

Olympus Recalls Sphincterotome Due to Deformation Risk

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

Philips Recalls IQon Spectral CT Over Potential Rotor Hazards

Philips North America Issues Recall for Spectral CT Due to Fastener Hazard

Philips North America recalled 283 Spectral CT units on January 7, 2026. Fasteners in the device may not be torqued to specification, posing a risk of unsecured rotor parts. While no incidents have been reported, potential safety hazards exist.

Medline Convenience Kits Recalled Due to Sterility Concerns