Medline recalls Centurion Sterile Weitlaner Retractor 3x4 Prong models with specific lot numbers due to potential puncture through sterile packaging. Affected users should check their product details.
Three is the potential for the retractors to puncture through the sterile packaging.
Medline is recalling Centurion Sterile Weitlaner Retractor 3x4 Prong surgical retractors because they might puncture the sterile packaging. This could lead to contamination during medical procedures. The recall affects specific lot numbers produced between 2020 and 2024.
The retractors could puncture the sterile packaging during use, potentially contaminating the surgical field. This risk occurs if the retractor is not properly secured within its packaging before use. The hazard is specific to the packaging integrity and not a direct injury risk.
Surgical professionals and hospitals using the Centurion Sterile Weitlaner Retractor 3x4 Prong with the listed lot numbers are affected. The risk is low as the hazard involves potential packaging puncture rather than immediate injury.
Check for lot numbers: 2020061990, 2020070990, 2020110490, 2020111090, 2021082590, 2021121490, 2022062890, 2022110190, 2022121990, 2023032290, 2023032390, 2023092590, 2024050790, 2024053090, 2024062490, 2024070190. The product is a surgical retractor sold by Medline.
Look for the lot numbers listed in the recall: 2020061990 through 2024070190.
The Centurion Sterile Weitlaner Retractor 3x4 Prong could puncture the sterile packaging, potentially contaminating the surgical field.
Check the lot number on your product; affected lots are listed as 2020061990 through 2024070190.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1766-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1766-2025 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.
