MEDLINE recalls alcohol swabsticks 3-pack with possible weak seal causing sterility breaches. Affected units sold in 2023 with specific lot numbers. Consumers should check product code and lot numbers for recall.
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
MEDLINE is recalling alcohol swabsticks 3-packs that may have a weak seal, risking contamination of sterile contents. This could lead to infections if the seal fails during use, though the failure isn't always detectable by users.
The swabsticks may have a weak seal that could breach sterility if the seal fails. This failure might not be noticeable to users, potentially leading to contaminated contents during medical or cleaning procedures.
Users of MEDLINE alcohol swabsticks 3-packs with lot number 2023071290 are affected. Healthcare workers and home users who rely on these swabs for cleaning or medical procedures are most at risk.
Check for product code DYNDA2723 on the packaging. The affected lot number is 2023071290 (not distributed). This product was sold in 2023 with specific case and individual lot numbers.
Look for product code DYNDA2723 on the packaging to confirm if it's affected.
Confirm the lot number is 2023071290 (not distributed) to identify affected units.
The recall indicates a potential weak seal that could breach sterility, but the product is still safe to use if the seal remains intact. However, users should check for the affected lot number.
Check the product code DYNDA2723 and lot number 2023071290 (not distributed) on the packaging.
The recall does not specify a remedy, so affected units should be checked for the lot number and disposed of if confirmed affected.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-1455-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-1455-2024 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.
