# FDA recall Z-2278-2019

> **Pega Medical Inc.** · Class II · device recall initiated 2019-05-29.

## Product

SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System

## Reason for recall

Handle could jam with the Driver due to the detachment of an internal Connector Ring.

## Distribution

CA, DE, FL, IL, NC, NE, NY and TN

## Key facts

- **Recall number:** Z-2278-2019
- **Recalling firm:** Pega Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-29
- **Report date:** 2019-08-21
- **Termination date:** 2021-01-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Laval, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2278-2019

## Citation

> AI Analytics. FDA recall Z-2278-2019. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2278-2019. Source: US FDA. Licensed CC0.

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