# FDA recall Z-0302-2020

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

## Product

Various Custom Devices, Item Nos. 32855090246  32855090252  32855090256  32855090265  32855090266  32855090270  32855090287  32855090290  32855090291  32855090297  32855090302  32855090317  32855090318  32855090319  32855090327  32855090329  32855090334  32855090336  32855090339  32855090348  32855090351  32855090352  32855090353  32855090354  32855090368  32855090369  32855090375  32855090376  32855090395  32855090396  32855090402  32855090409  32855090414  32855090434  32855090437  32855090439  32855090448  32855090450  32855090465  32855090484  32855090496  32855090497  32855090498  32855090501  32855090507  32855090512  32855090519  32855090520  32855090531  32855090543  32855090576  32855090585  32855090586  32855090593  32855090598  32855090599  32855090609  32855090615  32855090622  32855090628  32855090636  32855090637  32855090638  32855090640  32855090658  32855090659  32855090661  32855090715  32855090734  32855510763  32855510796  32855510797  32855510799  32855510800  3285

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0302-2020
- **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-0302-2020

## Citation

> AI Analytics. FDA recall Z-0302-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0302-2020. Source: US FDA. Licensed CC0.

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