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

Recall Z-0500-2025 — Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 280mm PM10.0-80B305 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 305mm PM10.0-80B335 PRECICE MAX Antegrade Fe

U.S. FDA — Device Enforcement · United States · 2024-09-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0500-2025
Date of alert: 2024-09-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: NuVasive Specialized Orthopedics, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00195377150929

Reported risk: Due to potential issues with design, manufacturing and documentation issues related to the validation of the affected products/devices.

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.

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.

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