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

Recall Z-0596-2018 — Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PPK implantable components into the medical knee compartment during unicondylar knee replacement.

U.S. FDA — Device Enforcement · United States · 2017-08-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0596-2018
Date of alert: 2017-08-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Biomet, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 42539909100

Reported risk: Potential for the Persona Partial Knee Impactor Pad to fracture.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.

Recall Z-0596-2018 — Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PPK implantable components into the medical knee compartment during unicondylar knee replacement.

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