CLASS II ONGOING Device recall · Reported 22 Apr 2026 · FDA Enforcement Report
Centurion Circumcision Kit, Medline Kit Number recalled
Medline Industries is recalling Centurion Circumcision Kit, Medline Kit Number, distributed nationwide in the US. The recall was initiated on 16 Mar 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1824-2026
- FDA event ID
- 98626
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 16 Mar 2026
- FDA classified
- 16 Apr 2026
- Reported
- 22 Apr 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Sterility
- Device type
- Other Medical Devices
Timeline
| 16 Mar 2026 | Recall initiated by company | |
| 16 Apr 2026 | Classified by FDA | +31 days |
| 22 Apr 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Where it was distributed
US Nationwide distribution in the state of South Carolina.
Questions about this recall
Why was it recalled?
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
Which lots are affected?
Medline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, Lot Number 25KLA002
Where was it sold?
US Nationwide distribution in the state of South Carolina.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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