Health & Personal Care
HIGH
FDA DEVICE
Medline Convenience Kits Recalled Over Sterility Concerns
Medline Industries, LP
Medline has
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DEVICE
Medline Drape Pack Recalled Over Sterility Concerns
Medline Industries recalled 72 units of Drape Pack-Choice, Model DYNJ63118A, on January 7, 2026. Calibration issues in sterilization equipment may compromise product sterility. Patients and healthcare providers should stop using the device immediately.
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
FDA DEVICE
Medline Surgical Kits Recalled Over Sterility Concerns
Medline Industries recalled 82,597 surgical kits on January 7, 2026, due to issues with sterilization calibration. The defect may compromise sterility assurance levels of the products. Healthcare providers and patients should stop using these kits immediately.
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls Surgical Convenience Kits Over Sterility Issues
Medline Industries recalled 39,315 surgical convenience kits on January 7, 2026. Calibration issues in sterilization equipment may compromise the sterility of these devices. Healthcare providers and patients should stop using these products immediately.
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
FDA DEVICE
CleverCut Sphincterotome V Recalled Due to Deformation Risk
CleverCut recalled 72,023 Single Use 3-Lumen Sphincterotome V devices on January 7, 2026. The devices may deform and lose performance due to a manufacturing issue. 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 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 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
Philips Recalls Spectral CT 7500 Over Fastener Issues
Philips North America recalled three Spectral CT 7500 units on January 7, 2026. The recall affects models with potential fastener issues that could lead to unsecured rotor parts. Patients and healthcare providers should stop using the device immediately.
Philips North America
As part
Health & Personal Care
HIGH
FDA DEVICE
Medline Surgical Kits Recalled Over Sterility Concerns
Medline Industries recalled 9,051 surgical kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple model numbers and poses a high hazard risk. Patients and healthcare providers should stop using these products immediately.
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Medline Convenience Kits Recalled Due to Sterilization Issues
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Medline Convenience Kits Recalled Due to Sterility Issues
Medline Industries, LP
Medline has
Tag Statistics
Total Recalls
2,756