# FDA recall Z-0323-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-10-10.

## Product

Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011  00585001201  00585001202  00585001301  00585001302  00585003038  00585003214  00585003217  00585003219  00585003238  00585003246  00585004445  00585004455  00585004465  00585004603  00585004604  00585004605  00585004606  00585004608  00585004610  00585004612  00585004614  00585004616  00585004618  00585004620  00585004622  00585004635  00585004645  00585004655  00585004808  00585004809  00585004820  00585204209  00585204217  00585205009  00585205010  00585205011  00585205012  00585205013  00585205014  00585205015  00585205016  00585205017  00585205018  00585205019  00585205209  00585205210  00585205211  00585205212  00585205213  00585205214  00585205215  00585205216  00585205217  00585205218  00585205219  00585205412  00585205413  00585205414  00585205415  00585205416  00585205417  00585205418  00585205419  00585207009  00585207010  00585207011  00585207012  00585207013  00585207014  00585207015  00585207016  0058520

## Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0323-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-10
- **Report date:** 2019-11-13
- **Termination date:** 2020-05-19

- **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-0323-2020

## Citation

> AI Analytics. FDA recall Z-0323-2020. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0323-2020. Source: US FDA. Licensed CC0.

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