Medline recalls Centurion retractor kits with weak seals that may breach sterility. Affected kits include ST7185 and RR602 models from specific lot numbers. Consumers should check product labels for recall details.
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 certain Centurion retractor kits due to a weak seal that could breach sterility if the seal fails. This risk is serious for medical procedures where sterility is critical, as the failure may not be detectable by all users.
The retractor kits have a weak seal that might break during use, leading to contamination of sterile contents. This breach could cause infections in patients if the seal fails and isn't detectable by all users.
Medical professionals using these retractor kits during surgeries or procedures are most at risk. Patients undergoing surgery with these kits could face infection if the seal fails.
Check for labels indicating STERILE 6-1/2" SENN RETRACTOR (ST7185) or STERILE RAGNELL RETRACTOR (RR602). The product codes 66795 and 67525 with specific lot numbers from 2023 are affected.
Look for the product codes 66795, 67525, or 37535 with the listed lot numbers on the packaging.
The recall is due to a weak seal in the retractor kits that may breach sterility if the seal fails, which could lead to infections during medical procedures.
Check for labels with product codes 66795, 67525, or 37535 and lot numbers from 2023 (e.g., 2023030190, 2023052390).
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1434-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1434-2024 from Medline Industries. 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.
