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

Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002) — recall Z-1874-2018

U.S. FDA — Device Enforcement · United States · 2018-03-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1874-2018
Date of alert
2018-03-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Epic Extremity, LLC
Product category
device
Product type
Devices
Reported risk: There is an error in the caddy artwork that misidentifies a specific plate and screw.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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