Medline recalls specific medical procedure kits due to a slight dimensional variation that may cause difficulty fitting into outer canisters. Affected kits include models with reference numbers DYNJ909171A, DYNJ905510D, DYNJ902388L, and DYNJ908566.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling certain medical procedure kits that may have a slight dimensional variation, making them harder to fit into outer canisters. This issue could lead to improper use during medical procedures, though it does not pose a direct safety risk.
The kits have a slight dimensional variation that can cause difficulty fitting into the outer canister. This may lead to improper use during medical procedures, but it does not cause injury or damage to the user.
Healthcare professionals using the recalled Medline medical procedure kits are most at risk. Patients using these kits during procedures may be affected if the kits do not fit properly.
Check for the reference numbers DYNJ909171A, DYNJ905510D, DYNJ902388L, or DYNJ908566 on the kit labels. The lot numbers listed in the recall notice also help identify affected units.
Look for the reference numbers DYNJ909171A, DYNJ905510D, DYNJ902388L, or DYNJ908566 on the kit labels.
No, the recall does not require stopping use. The issue is a minor fit problem that does not pose a safety risk.
Check the reference numbers on the kit labels: DYNJ909171A, DYNJ905510D, DYNJ902388L, or DYNJ908566.
The recall does not specify a remedy, so no action is required beyond checking the labels.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2711-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2711-2024 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.
