---
title: "EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base — FDA record Z-0276-2023 | Is It on Recall"
description: "One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 191671"
url: https://isitonrecall.com/recall/fda-device-z-0276-2023-evolution-mp-tibial-bases-size-7-left-ref-etpkn7sl-knee-tibial-base/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base — FDA record Z-0276-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 28, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: MicroPort Orthopedics Inc.
- **Quantity**: 22 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0276-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0276-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 0 0192629 08293 9, Lot 1916715 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Feb 22, 2023
- **Recall initiation date**: Oct 28, 2022
- **Center classification date**: Nov 22, 2022
- **Termination date**: Sep 10, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0276-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MicroPort Orthopedics Inc. records](https://isitonrecall.com/brand/microport-orthopedics-inc/)