Medline Industries has recalled 3,578,805 units of its sterile saline wound wash due to potential sterility assurance issues. The recall, effective January 5, 2026, affects products distributed worldwide, including in the U.S. Consumers should stop using the product immediately.
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
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 Sterile Saline Wound Wash is designed for wound cleansing and irrigation. Consumers typically use it for minor cuts, scrapes, and other skin injuries to promote healing.
The recall is due to the manufacturer potentially failing to meet sterility requirements. This can lead to contamination, which poses a risk of infection when used on wounds.
This recall is not part of a broader industry pattern.
Consumers may face health risks if contaminated products were used. Stopping use and replacing the product is critical to prevent infections.
The model number can often be found on the label of the can or packaging.
Expect 4-6 weeks for the refund process after returning the product.
Keep receipts and any correspondence with Medline regarding the recall for your records.
The recalled product is Medline Sterile Saline Wound Wash, Model Number MDSALINE7. It comes in a 7.1 FL OZ (210 mL) spray can. The product was distributed worldwide, including the U.S., Bahamas, Bermuda, and Cayman Islands.
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