# FDA recall Z-0334-2020

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

## Product

Metasul Taper Liner, various sizes, Item Nos. 00877000528  00877000628  00877000732  00877000832  00877000936  00877001036  00877001140  00877001240  00877001340  00877001440  00877001540  00877001640  00877001740  00877001840  00877001940  00877002040  00877002140  00877002240  00877002340

## Reason for recall

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

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0334-2020
- **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-0334-2020

## Citation

> AI Analytics. FDA recall Z-0334-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0334-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*