# FDA recall Z-0318-2020

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

## Product

Various Hip Joint Replacement Systems, Item Nos. 00151504232  00151504432  00151504636  00151504836  00151505040  00151505240  00151505444  00151505644  00151505848  00151506048  00151506248  00151506448  00151506648  00400500060  00401000038  00401000040  00401000041  00401000042  00401000043  00401000044  00401000045  00401000046  00401000047  00401000048  00401000049  00401000050  00401000051  00401000052  00401000053  00401000054  00401000055  00402100857  00402100863  00402101243  00402101244  00402200040  00402200042  00402200051  00402200057  00408801106  00408801206  00408801226  00408801236  00408801306  00408801326  00408801336  00408801356  00408801376  00408801406  00408801426  00408801436  00408801456  00408801476  00408801506  00408801526  00408801536  00408801556  00408801576  00408801606  00408801626  00408801636  00408801656  00408801706  00408801806  00455500700  00455501001  00455502000  00455502001  00455503000  00455503001  00455504001  00500103800  00500103900  00

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0318-2020
- **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-0318-2020

## Citation

> AI Analytics. FDA recall Z-0318-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0318-2020. Source: US FDA. Licensed CC0.

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