Medline recalls Centurion scalpel handle kits with weak seals that may breach sterility. Affected kits have specific product codes and lot numbers. Stop using if you have these items.
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 scalpel handle kits that may have weak seals causing sterility breaches. This could lead to infections if the seal fails during use, even if users don't notice the problem.
The scalpel handle kits may have a weak seal that can break, allowing contamination of the sterile blades. This breach might not be noticeable to users, increasing infection risks during procedures.
Healthcare professionals using these scalpel kits for surgical procedures are most at risk. Patients could face infections if the seal fails during surgery.
Check for product codes 66825 (for handles) or I68290 (for blades) with specific lot numbers: 2023091990, 2023111590 for handles and 2023100690 for blades.
Look for product codes 66825 or I68290 with lot numbers 2023091990, 2023111590 (handles) or 2023100690 (blades).
If you have the recalled kits, stop using them immediately to prevent potential infection risks.
Product codes 66825 (for scalpel handles) and I68290 (for blades) with specific lot numbers: 2023091990, 2023111590 for handles and 2023100690 for blades.
The recall is due to a weak seal that may breach sterility of the contents, potentially leading to infections if the seal fails during use.
The recall record does not specify a return process or remedy, 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-1436-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1436-2024 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.
