Centurion CIRCLAMP W/1 — Class II medical device recall Z-0121-2020
Terminated recall by Centurion Medical Products Corporation, reported 2019-10-16, distributed nationwide. A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to r
| Recall number | Z-0121-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2019-08-28 |
| Classified | 2019-10-10 |
| Reported by FDA | 2019-10-16 |
| Terminated | 2020-07-23 |
| Distributed | Nationwide (US) |
| Quantity | 204 units |
| Lot numbers | 2019061201 |
Product
Centurion CIRCLAMP W/1.3 CM BELL-single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. ReOrder: 330CR
Reason for recall
A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0121-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.