# FDA recall Z-0276-2023

> **MicroPort Orthopedics Inc.** · Class II · device recall initiated 2022-10-28.

## Product

EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base

## Reason for recall

One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.

## Distribution

International Distribution to countries of: Germany, Italy, France, Belgium, Austria, Greece, Romania, Japan, and P.R. China.

## Key facts

- **Recall number:** Z-0276-2023
- **Recalling firm:** MicroPort Orthopedics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-28
- **Report date:** 2023-02-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0276-2023

## Citation

> AI Analytics. FDA recall Z-0276-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0276-2023. Source: US FDA. Licensed CC0.

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