Health & Personal Care Recalls

Medline Medical Kits Recalled Due to High Hazard Risk

Medline Dialysis Kits Recalled Over Risk of Fluid Leakage

Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.

Medline Recalls Dialysis Dressing Change Kits Over High Hazard

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Medline Recalls Convenience Kits Over Sterility Concerns

Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.

Medline Recalls Convenience Kits Over Sterility Issues

Olympus Medical Device Recalled Over Deformation Risk

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

Olympus Recalls Sphincterotome Over Deformation Risk

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

Olympus Recalls Sphincterotome Over Performance Risks

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

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 Recalls Sphincterotome Over Performance Risks

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 V Due to Deformation Risk

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

Olympus Sphincterotome Recalled Due to Performance Risks

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 Single Use 3-Lumen Sphincterotome Due to Performance 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 Hazardous Deformation Risk

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

Olympus Recalls Sphincterotome Due to Potential Deformity Hazard

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.