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

Recall Z-1811-2014 — Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System.

U.S. FDA — Device Enforcement · United States · 2014-05-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1811-2014
Date of alert
2014-05-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ebi, Llc
Product category
device
Product type
Devices
Reported risk: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument tip failure.
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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