141 recalls found for Medline Industries, LP. Check if any of your products are affected.
Medline recalled 108,971 units of Puracol MSC8522 and Puracol Plus MSC8622EP collagen wound dressings nationwide in the United States, with distribution to Mexico and Panama. Elevated endotoxin levels were identified in affected lots. Stop using the dressings and follow recall instructions provided by Medline or your healthcare provider.
The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
Medline Industries recalled 150 dialysis convenience kits on January 8, 2026, due to silicone seal defects. Affected kits may obstruct fluid paths and risk exposure to biological contaminants.
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 Industries recalled 1,212 kits containing Tego Connectors on January 8, 2026. The recall stems from issues with silicone seals that may cause occluded fluid paths. Users may experience delays in therapy or exposure to contaminants due to this defect.
Medline Industries recalled 516 medical kits on January 8, 2026, due to issues with Tego Connectors. The silicone seal may tear or dome, posing a high risk of therapy interruption and exposure to contaminants. Healthcare providers must stop using these devices immediately and follow recall instructions.
Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.
Medline Industries recalled 31,848 dialysis dressing change kits on January 8, 2026. The recall follows reports of defective silicone seals on Tego Connectors that may occlude fluid paths. This defect can delay therapy and expose patients to biological contaminants.
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 Industries recalled 7,725 surgical kits on January 7, 2026, due to potential sterility issues. Calibration problems with sterilization equipment may compromise the sterility assurance level. Healthcare providers and patients should stop using these kits immediately.
Medline Industries recalled 32 units of Convenience Kits on January 7, 2026. Issues with sterilization equipment calibration may compromise device safety. Users should stop using the products immediately and follow recall instructions.
Medline recalled 108 units of its Convenience Kits, model DYKMBNDL200A, due to calibration issues affecting sterility. The recall, issued on January 7, 2026, impacts products distributed worldwide. Healthcare providers and patients must stop using the kits immediately.
Medline Industries, LP recalled 684 medical convenience kits on January 7, 2026. The recall affects the LVAD Driveline Tray and the KIT Surg Onc Insert Cent. Venou due to calibration issues impacting sterility. Health providers and patients should stop using these products immediately.
Medline Industries recalled 23,238 convenience kits on January 7, 2026. The recall affects the BAPTIST FLOYD ENDO GI KIT and GI LAB OTHER ENDO KIT due to calibration issues that may compromise sterility. Patients and healthcare providers should stop using the products immediately.
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 Industries recalled 2,236 dental packs on January 7, 2026, due to calibration issues affecting sterilization. The recall impacts products distributed worldwide, raising safety concerns for healthcare providers. Consumers should stop using the recalled items immediately and follow manufacturer instructions.
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 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.