Medline Centurion Sterile CirClamp Recall: Packaging Holes Risk Contamination
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.
Lower-risk recall
Product has been identified as having holes in the packaging.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/54126-medline-centurion-sterile-circlamp-recall-packaging-holes-risk-contamination.
Source Summary by GovInfoNow · govinfonow.com/recall/54126-medline-centurion-sterile-circlamp-recall-packaging-holes-risk-contamination · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0133-2025
Cite this page
“Medline Centurion Sterile CirClamp Recall: Packaging Holes Risk Contamination.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54126-medline-centurion-sterile-circlamp-recall-packaging-holes-risk-contamination. Based on FDA recall #Z-0133-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0133-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Product Details
Identify your product by checking the reorder number and lot numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of India and Panama.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 57 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have an affected product?
Contact Medline directly to confirm your product's status and follow their guidance for next steps.
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Where this comes from
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.
- Official source: FDA Recall #Z-0133-2025 (September 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0133-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.