Medline recalls sterile saline wound wash products due to potential failure to meet sterility standards. Affected items may cause infection if used improperly.
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.
Medline is recalling sterile saline wound wash products because they might not meet sterility requirements. Using these products could lead to infections if they are not properly sterile.
The saline products may not meet sterility standards, meaning they could be contaminated. This contamination could lead to infections if used on open wounds or during medical procedures.
People who use sterile saline wound wash products for medical care. Those with open wounds or surgical procedures are at higher risk.
Check for the model number MDSALINE7 on the product label. The product was sold in 2019 with lots 10193489089356 (each) and 10193489089353 (case).
Look for the model number MDSALINE7 on the product label.
The recall states the product may not meet sterility standards, so it is not recommended for use until the recall is resolved.
The recall does not specify a remedy, so check with Medline for guidance.
Look for the model number MDSALINE7 on the product label and check the lot numbers 10193489089356 (each) or 10193489089353 (case).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1431-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1431-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.