Medline recalls 15 types of Centurion Sterile CirClamps due to holes in packaging that could lead to contamination. Affected products include specific reorder numbers and lot numbers. Consumers should check their product details and contact Medline for guidance.
Product has been identified as having holes in the packaging.
Medline is recalling 15 different types of Centurion Sterile CirClamps because the packaging has holes. This could allow contamination of the medical devices, making them unsafe for use.
The packaging has holes that could allow contaminants to enter the sterile product. This poses a risk of contamination during medical procedures, but the hazard is not immediate or life-threatening.
Healthcare professionals and medical facilities that use these specific Centurion Sterile CirClamps are likely affected. The risk is low as the hazard involves packaging issues rather than direct product failure.
Check the product name and reorder number (e.g., Centurion Sterile CirClamp, Reorder #200CR). Look for specific lot numbers listed in the recall notice or the UDI-DI codes provided.
Identify your product by checking the reorder number and lot numbers listed in the recall notice.
The packaging has holes that could allow contaminants to enter the sterile product, posing a risk of contamination during medical procedures.
Check the reorder number and lot numbers listed in the recall notice. Affected products include specific Centurion Sterile CirClamps with reorder numbers like #200CR, #210CR, and others.
Contact Medline directly to confirm your product's status and follow their guidance for 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-0133-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0133-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
