# FDA recall Z-1875-2018

> **Epic Extremity, LLC** · Class II · device recall initiated 2018-03-20.

## Product

Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking Screw (2001-27XX-N & 2001-35XX-N)

## Reason for recall

There is an error in the caddy artwork that misidentifies a specific plate and screw.

## Distribution

The products were distributed to the following US states: FL, PA, and VA.

## Key facts

- **Recall number:** Z-1875-2018
- **Recalling firm:** Epic Extremity, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-20
- **Report date:** 2018-05-23
- **Termination date:** 2019-04-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cranberry Twp, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1875-2018

## Citation

> AI Analytics. FDA recall Z-1875-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1875-2018. Source: US FDA. Licensed CC0.

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