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

Recall Z-0981-2025 — stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during neurosurgery

U.S. FDA — Device Enforcement · United States · 2023-06-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0981-2025
Date of alert
2023-06-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04546540467775
Reported risk: There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
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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