# FDA recall Z-0312-2020

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

## Product

Universal Locking Plates Sterile, Item Nos.   47492800207  47492800303  47492800402  47492800403  47492800407  47492800502  47492800503  47492800507  47492800603  47492800607  47492800613  47492800702  47492800703  47492800707  47492800802  47492800803  47492800807  47492800813  47492800902  47492800907  47492801002  47492801007  47492801013  47492801207  47492801213  47492801413  47492801607  47492801613  47492801702  47492801802  47492801813  47492801902  47492802002  47492802013  47493600313  47493600403  47493600407  47493600413  47493600503  47493600507  47493600513  47493600603  47493600607  47493600613  47493600703  47493600707  47493600713  47493600803  47493600807  47493600813  47493600907  47493600913  47493601003  47493601007  47493601013  47493601113  47493601203  47493601207  47493601213  47493601313  47493601403  47493601407  47493601413  47493601513  47493601607  47493601613  47493601813  47493602007  47493602013  47493602213  47493603305  47493603306  47493603405  47493

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0312-2020
- **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-0312-2020

## Citation

> AI Analytics. FDA recall Z-0312-2020. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-0312-2020. Source: US FDA. Licensed CC0.

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