# FDA recall Z-0121-2020

> **Centurion Medical Products Corporation** · Class II · device recall initiated 2019-08-28.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-0121-2020
- **Recalling firm:** Centurion Medical Products Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-28
- **Report date:** 2019-10-16
- **Termination date:** 2020-07-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Williamston, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0121-2020

## Citation

> AI Analytics. FDA recall Z-0121-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0121-2020. Source: US FDA. Licensed CC0.

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