Medline recalls Centurion Sterile Weitlaner retractors that may puncture sterile packaging. Affected units have specific lot numbers and UDI/DI codes. Stop using and contact Medline for replacement.
Three is the potential for the retractors to puncture through the sterile packaging.
Medline is recalling Centurion Sterile Weitlaner retractors that could puncture the sterile packaging during use. This poses a risk of contamination or infection if the packaging is compromised. Affected units have specific lot numbers and UDI/DI codes.
The retractors may puncture through the sterile packaging during use, potentially contaminating the surgical site. This could lead to infection or other complications if the packaging is compromised.
Surgical staff and medical professionals who use these retractors during procedures are most at risk. Patients could be exposed to infection if the sterile packaging is punctured.
Check for the UDI/DI code 10653160379867 (each) or 00653160379860 (case) and lot numbers listed in the recall notice. The product is sold under the brand name Centurion Sterile Weitlaner Retractor.
Immediately stop using the recalled retractors as they may puncture sterile packaging.
Reach out to Medline Industries for a replacement or refund using the provided lot numbers and UDI/DI codes.
The retractors may puncture through the sterile packaging, potentially causing contamination or infection.
Check for the UDI/DI code 10653160379867 (each) or 00653160379860 (case) and lot numbers listed in the recall notice.
Immediately stop using it and contact Medline Industries for a replacement or refund.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1765-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1765-2025 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.
