Medline Centurion Circumcision Kit Not Sterile: Recall for Risk of Infection
Medline recalls Centurion Circumcision Kit (SKU CIT7050F) due to potential lack of sterilization, risking infection. Affected units sold with specific lot numbers.
Lower-risk recall
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
Contact the company
What happened, in plain English
Medline is recalling certain Centur: Circumcision Kits because some were distributed without proper sterilization. Using these kits could lead to infection since they are not sterile. Read more at govinfonow.com/recall/49722-medline-centurion-circumcision-kit-not-sterile-recall-for-risk-of.
Source Summary by GovInfoNow · govinfonow.com/recall/49722-medline-centurion-circumcision-kit-not-sterile-recall-for-risk-of · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1824-2026
Cite this page
“Medline Centurion Circumcision Kit Not Sterile: Recall for Risk of Infection.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/49722-medline-centurion-circumcision-kit-not-sterile-recall-for-risk-of. Based on FDA recall #Z-1824-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1824-2026%22&limit=1).
Why it’s dangerous
The kits were distributed without the required sterilization process, meaning they are not sterile. This can lead to infection if used for circumcision procedures since the kits are meant to be sterile.
Who’s affected
People who purchased the Centurion Circumcision Kit (SKU CIT7050F) with lot number 25KLA002 or UDI/DI numbers 10198459536656/40198459536657 are affected. Those using the kit for medical procedures are at higher risk.
How to tell if you have this one
Check the kit's Medline SKU number (CIT7050F) and lot number (25KLA002) or UDI/DI numbers (10198459536656 for individual, 40198459536657 for case).
- Brand
Medline- Category
Medical device
What to do — step by step
Check Kit Details
Look for the lot number 25KLA002 or UDI/DI numbers 10198459536656 (individual) or 40198459536657 (case) on the kit.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of South Carolina.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 37 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.
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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-1824-2026 (March 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1824-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 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.