Health & Personal Care Recalls

Medline Recalls Convenience Kits Due to Sterility Risks

Medline Dental Pack Recalled Over Sterility Concerns

Medline Recalls Arthroscopy Kits Over Sterility Concerns

Medline Industries recalled 175 arthroscopy kits on January 7, 2026. Calibration issues with sterilization equipment may impact product sterility. Patients and healthcare providers should stop using the devices immediately.

Medline Convenience Kits Recalled Due to Sterility Issues

Medline Industries recalled 30,958 convenience kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Healthcare providers and patients must stop using these products immediately.

Medline Surgical Drapes Recalled Over Sterility Issues

Medline Industries recalled 14.9 million surgical drapes on January 7, 2026. Calibration issues with sterilization equipment may impact sterility assurance levels. Patients and healthcare providers must stop using these products immediately.

Medline Recalls Convenience Kits Over Sterility Assurance Issues

Medline Industries recalled 240 units of convenience kits on January 7, 2026. Calibration issues with sterilization equipment may impact product safety. Patients and healthcare providers should stop using these devices immediately.

Medline Recalls Surgical Kits Over Sterility Assurance Issues

Medline Surgical Kits Recalled Over Sterility Assurance Issues

Medline Industries recalled 4,853 surgical kits on January 7, 2026 due to potential sterility issues. Calibration problems with sterilization equipment could affect safety. Patients and providers must stop using these kits immediately.

Medline Recalls Convenience Kits Due to Sterility Concerns

Medline Industries, LP recalled 551 units of convenience kits on January 7, 2026. Calibration issues in sterilization equipment may affect product sterility. Healthcare providers and patients must stop using the kits immediately.

Medline Surgical Kits Recalled Over Sterility Concerns

Medline Industries recalled 2,740 surgical kits on January 7, 2026. Calibration issues with sterilization equipment jeopardize the sterility assurance level of the products. Healthcare providers and patients must stop using these devices immediately.

Medline Convenience Kits Recalled Over Sterility Concerns

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 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 PPE Kits Recalled Due to Sterilization Issues

Medline Recalls Surgical Gowns Due to Sterility Risk

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.

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 Recalls Sphincterotome Due to Deformation Risk

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

Olympus Recalls Sphincterotome Due to Deformation Risk

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

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.