Medline recall covers 104,004 Medcrest Surgical Gowns sold nationwide and internationally due to premature fabric delamination risk. Delamination can delay patient care in surgery and raise infection risk. Stop using the affected gowns and follow the manufacturer’s recall instructions immediately.
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.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
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Medline Medcrest Surgical Gowns are disposable gowns used in surgical settings. They are distributed nationwide in the US and internationally.
Fabric delamination can occur with laundering, potentially delaying surgery and increasing infection risk if used.
This recall is not identified as part of a broader industry pattern in the provided data.
Hospitals may need to identify and replace affected gowns to prevent delays and infection risk during procedures.
Look on the packaging, labeling, and cuff tags for model numbers and UDI-DI identifiers.
Recall remedies are issued by the manufacturer; processing times vary and may take weeks.
Keep a copy of the recall notice, take photos of labels and tags, and document all correspondence with the supplier.
Model numbers listed in recall: MDTGXC4J5XL, MDTGXC4JL, MDTGXC4JXL, MDTGXC4JXXL, MDTGXP4JL, MDTGXP4JXL, MDTGXP4JXXL, MDTL1002862EF, MDTZ1000893AJ. Distribution: Domestic distribution nationwide in the United States; international distribution to Panama, United Arab Emirates, Virgin Islands, Saudi Arabia, India, Chile, and Canada. Quantity: 104,004 units. Sold at: Unknown. Price: Unknown.
No injuries or incidents have been reported.
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