Medline recalls Centurion surgical kits with weak seals that may breach sterility. Affected kits have specific product codes and lot numbers. Stop using if you own these kits to prevent infection risks.
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 Centurion manual surgical kits that may have weak seals causing sterility breaches. This could lead to infections if the seal fails during use, which might not be noticeable to users.
The kits may have weak seals that can fail without being detected by users. If the seal breaks, the sterile contents could become contaminated, increasing infection risks during medical procedures.
Surgical professionals and healthcare facilities using the Centurion kits with the specified product codes and lot numbers are most at risk. Patients receiving procedures with these kits could face infection risks.
Check for product codes: 15MLVLCP for the 15ML sampling tube with cap, and MG912ST for the sterile 9x12 reclosable bag. Lot numbers 2023102790 and 2023022190 are associated with these kits.
Look for product codes 15MLVLCP or MG912ST on the kits to identify affected units.
If you have the affected kits, stop using them immediately to prevent potential contamination.
The recall is due to a potential weak seal in the surgical kits that could breach sterility if the seal fails, which might not be detectable by users.
Check for product codes 15MLVLCP or MG912ST and lot numbers 2023102790 or 2023022190 on the kits.
Stop using the kits immediately if you have them, as they may cause contamination risks during procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1448-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1448-2024 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.
