# FDA recall Z-2090-2019

> **Encore Medical, Lp** · Class II · device recall initiated 2018-09-19.

## Product

Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.

## Reason for recall

Manufacturing error, the drill bit shaft is unable to  properly capture the drill bit pin. Failure of the drill bit  shaft to capture the drill bit pin could result in the drill bit coming loose which could result in a  delay in surgery or adverse patient reaction resulting in a revision surgery.

## Distribution

US ( MS, NY, MO, OK, UT, AZ)

## Key facts

- **Recall number:** Z-2090-2019
- **Recalling firm:** Encore Medical, Lp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-09-19
- **Report date:** 2019-08-07

- **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-2090-2019

## Citation

> AI Analytics. FDA recall Z-2090-2019. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2090-2019. Source: US FDA. Licensed CC0.

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