# FDA recall Z-1306-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2017-10-25.

## Product

A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887868044670989403

## Reason for recall

The drill guides were manufactured with the incorrect color anodization.

## Distribution

Distributed in the following US States: AZ, MO, MT, NJ, NY, OH, TX, and WA. Distributed in Chile and Netherlands.

## Key facts

- **Recall number:** Z-1306-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-25
- **Report date:** 2018-04-11
- **Termination date:** 2020-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1306-2018

## Citation

> AI Analytics. FDA recall Z-1306-2018. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-1306-2018. Source: US FDA. Licensed CC0.

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