# FDA recall Z-3102-2017

> **Encore Medical, Lp** · Class II · device recall initiated 2017-08-04.

## Product

MODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers:    REF S-200956 - 5mm PIN, SIZE 46   REF S-200957 - 5mm PIN, SIZE 50  REF S-200958 - 5mm PIN, SIZE 58

## Reason for recall

It was reported that the models used to manufacture S-200956/958 had the wrong dimension used to create the spherical radius cutting surface. Device design allows a larger spherical radius cutting surface than intended.

## Distribution

OH, VA

## Key facts

- **Recall number:** Z-3102-2017
- **Recalling firm:** Encore Medical, Lp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-08-04
- **Report date:** 2017-09-06
- **Termination date:** 2023-06-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3102-2017

## Citation

> AI Analytics. FDA recall Z-3102-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-3102-2017. Source: US FDA. Licensed CC0.

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