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

Recall Z-1751-2014 — Stryker 2.0mm Round Fluted Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications including maxillofaci

U.S. FDA — Device Enforcement · United States · 2014-05-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1751-2014
Date of alert: 2014-05-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Instruments Div. of Stryker Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 13347017

Reported risk: There may be missing notches, partial notches or no notches at all in some Cutting Accessories that are used with the Elite" Attachments.

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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