# FDA recall Z-0326-2020

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

## Product

Various fixation systems and accessories, Item Nos. 00118100522  00118100527  00118100530  00118100532  00118100535  00118100537  00118100540  00118100542  00118100550  00118100552  00118100562  00118100565  00118100567  00118101022  00118101025  00118101027  00118101030  00118101032  00118101035  00118101037  00118101040  00118101042  00118101045  00118101047  00118101050  00118101052  00118101055  00118101057  00118101060  00118101522  00118101525  00118101527  00118101530  00118101532  00118101547  00118101552  00118101557  00118109006  00118109008  00118109010  00118109506  00118109510  00118113002  00118113003  00118113004  00118113005  00118113006  00118113008  00118113010  00118113012  00118113094  00118113502  00118113503  00118113504  00118113505  00118113506  00118113508  00118113510  00118113512  00118113514  00118113594  00118113595  00118114002  00118114003  00118114004  00118114005  00118114006  00118114008  00118114010  00118114012  00118114014  00118114094  00118114095 

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0326-2020
- **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-0326-2020

## Citation

> AI Analytics. FDA recall Z-0326-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0326-2020. Source: US FDA. Licensed CC0.

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