Medline Industries recalls 1.5L MED-SOFT Liner with 6mm x 1.8m tube due to slight dimensional variations causing increased difficulty fitting into 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 Industries is recalling 1.5L MED-SOFT Liner with 6mm x 1.8m tube because a slight dimensional variation makes it harder to fit into the outer canister. This could lead to improper use or damage if the liner doesn't fit correctly.
The liner has a slight dimensional variation that makes it more difficult to fit into the outer canister. This could lead to improper use or damage if the liner doesn't fit correctly, but it does not pose a risk of injury or serious harm.
Users of the 1.5L MED-SOFT Liner with 6mm x 1.8m tube who purchased it between specific dates and lot numbers. Those who have the product with the listed UDI/DI codes or lot numbers are most at risk.
Check the product for the UDI/DI code 40888277422279 on the package and 0888277DC265NSKX on the unit. Also look for lot numbers 670220512 through 670221009.
Verify the UDI/DI code on the package (40888277422279) and unit (0888277DC265NSKX), and check the lot numbers listed.
The product has a slight dimensional variation that makes it more difficult to fit into the outer canister, which could lead to improper use or damage.
Check the product for the UDI/DI code 40888277422279 on the package and 0888277DC265NSKX on the unit, and lot numbers 670220512 through 670221009. If you have these details, contact Medline Industries for further instructions.
No, the recall states this is a low-risk issue that does not pose a risk of injury or serious harm.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2697-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2697-2024 from Medline Industries. 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.
