Medline recalls 1.5L MED-SOFT LINER with 6mm x 3m tube for potential fit issues with outer canister. Affected units have specific lot numbers and UDI/DI codes.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling 1.5L MED-SOFT LINER products with 6mm x 3m tubes that may have slight dimensional variations causing difficulty fitting into outer canisters. This issue doesn't pose a safety risk but could lead to improper use.
The product has slight dimensional variations that may make it harder to fit into the outer canister. This could lead to improper use, but it does not cause injury or damage to the user.
Users of Medline's 1.5L MED-SOFT LINER with 6mm x 3m tubes, particularly those who use the product for medical purposes. Individuals with specific lot numbers or UDI/DI codes listed in the recall are most affected.
Check the product label for lot numbers: 670220505, 670220609, 670220621, 670220720, 670220804, 670220926, 670220928, 670221024, 670221115, 670221227, 670230109, 670230210, 670230424. Also look for UDI/DI codes: 40888277422286 (package) or 0888277DC265NSKX (unit).
Look for lot numbers listed in the recall: 670220505, 670220609, 670220621, 670220720, 670220804, 670220926, 670220928, 670221024, 670221115, 670221227, 670230109, 670230210, 670230424.
No, the recall is for potential fit issues with the outer canister, not a safety hazard.
Check the product label for lot numbers: 670220505, 670220609, 670220621, 670220720, 670220804, 670220926, 670220928, 670221024, 670221115, 670221227, 670230109, 670230210, 670230424.
The recall does not require action; the product is safe but may have fit issues.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2698-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2698-2024 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.
