Medline recalls Centurion surgical kits with weak seals that may breach sterility. Affected kits include specific sizes and lot numbers. Consumers should check product labels for the listed codes and serial numbers.
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 several Centurion manual surgical kits due to a potential weak seal that could breach sterility. This risk means the kits might not stay sterile if the seal fails, which could lead to infections during medical procedures.
The kits may have a weak seal that can fail without being detectable by users. If the seal breaks, the contents could become contaminated, increasing the risk of infection during medical procedures.
Healthcare professionals using these surgical kits for procedures like uterine dilation are most at risk. Patients undergoing such procedures with affected kits could face infection.
Check for product labels indicating the specific sizes and codes listed: HEGAR UTERINE DILATOR 11-12MM (HUD112ST), STERILE UTERINE DILATOR 1MM/2MM (HUD12ST), etc. Look for lot numbers like 2023032190 or 2023112990.
Look for the product codes and lot numbers listed in the recall notice to confirm if your kit is affected.
Reach out to Medline Industries for further assistance if you have the affected kits.
The recall includes Centurion manual surgical kits with specific sizes: HEGAR UTERINE DILATOR 11-12MM (HUD112ST), STERILE UTERINE DILATOR 1MM/2MM (HUD12ST), HEGAR UTERINE DILATOR 5-6MM (HUD56ST), HEGAR UTERINE DILATOR 9-10MM (HUD910ST), HANK UTERINE DILATOR 11" 7/8FR (I68920), and HANK UTERINE DILATOR 11" 13/14FR (I68930).
Check for the product codes and lot numbers listed in the recall notice, such as HUD112ST with lot number 2023032190 or HUD12ST with lot numbers 2023061690 and 2023112990.
The recall does not specify a remedy, so contact Medline Industries directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1450-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1450-2024 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.