Product Wiki · Recalls · U.S. FDA — Device Enforcement

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

U.S. FDA — Device Enforcement · United States · 2022-10-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0276-2023
Date of alert
2022-10-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MicroPort Orthopedics Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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