# FDA recall Z-0304-2020

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

## Product

NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009  0202263012  0202263015  0202263018  0202263021  0202263109  0202263112  0202263115  0202263118  0202263121  0202264009  0202264012  0202264015  0202264018  0202264021  0202264109  0202264112  0202264115  0202264118  0202264121  0202265010  0202265012  0202265014

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0304-2020
- **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-0304-2020

## Citation

> AI Analytics. FDA recall Z-0304-2020. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-0304-2020. Source: US FDA. Licensed CC0.

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