FDA recall, , Moderate risk
Medline CENTURION Circumcision Kit
The CENTURION Circumcision Kit was distributed without required sterilization and is not sterile.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, recalled the CENTURION Circumcision Kit because it was distributed without the required sterilization process and is therefore not sterile. The recall began March 16, 2026, and was added to the FDA's Enforcement Report on April 16, 2026.
The affected kits were distributed in South Carolina. The FDA classified the recall on April 16, 2026, and it was included in the agency's weekly enforcement report on April 22, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Match the SKU, UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
CENTURION Circumcision Kit
- SKU
- CIT7050F
- UDI-DI
- 10198459536656
- 40198459536657
- Lot code
- 25KLA002
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of South Carolina.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Sterility problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98626
- Recall number
- Z-1824-2026
- Quantity recalled
- 640 kits
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
