Medline recalls Centurion surgical kits with weak seals that could 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 leading to sterility breaches. This could cause infections if the seal fails during use, especially in medical settings where sterility is critical.
The kits may have a weak seal that can fail without being detectable by users. If the seal breaks, the contents could become contaminated, risking infections during surgery.
Healthcare professionals and surgical teams using these kits are most at risk. Patients undergoing procedures with these kits could face infection if the seal fails.
Check for product codes: I68905 (Allis Tiss FCP 10"), MNS11505 (Vaginal Repair Kit), MNS11545 (PTCA Add-on Kit), or SUT21355 (Instrument Set). Look for lot numbers from 2023012590 to 2023071390.
Identify kits with product codes I68905, MNS11505, MNS11545, or SUT21355.
Discontinue use immediately if you have the affected kits to prevent potential sterility breaches.
Affected product codes include I68905 (Allis Tiss FCP 10"), MNS11505 (Vaginal Repair Kit), MNS11545 (PTCA Add-on Kit), and SUT21355 (Instrument Set).
Check for lot numbers from 2023012590 to 2023071390 on the kit's packaging or label.
The recall does not specify a return process, so contact Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1443-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1443-2024 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.
