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

Recall Z-0699-2025 — EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component

U.S. FDA — Device Enforcement · United States · 2024-10-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0699-2025
Date of alert
2024-10-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MicroPort Orthopedics Inc.
Product category
device
Product type
Devices
Reported risk: Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect 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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.