High Risk Recalls

Medline Surgical Packs: 1) PACK,UNIVERSAL,ULTRAGARD,5/CS, Model Number: DYNJP1050UG; 2) PACK,SHOULDER,DRAPE,POUCH,10/CS, Model Number: DYNJP8401

Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035; 2) LVAD DRIVELINE TRAY, Model Number: DM1035A; 3) CENTRAL LINE DRESSING CHANGE TRAY, Model Number: DT8670A

Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A

See complete list in RES, exceeds character limit. Medline Surgical Gowns

Medline Convenience Kits: 1) KIT GENERAL CLOSURE, Model Number: DYKMBNDL200A

Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.;

If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.

Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY, Model Number: DYNDA2941A; 2) CHEST/BREAST-LF, Model Number: DYNJ83950; 3) HERNIA REPAIR TOTE, Model Number: DYNJ908337A; 4) HERNIA...

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.

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 Recalls Surgical Kits Over Sterility Concerns

Medline Recalls Convenience Kits Over Sterility Concerns