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

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar. — recall Z-0810-2013

U.S. FDA — Device Enforcement · United States · 2012-12-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0810-2013
Date of alert
2012-12-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mizuho OSI
Product category
device
Product type
Devices
Reported risk: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the aluminum plug may migrate out of the carbon fiber tube. If this occurs, the Orthopedic Table Spar may need to be replaced to ensure stability of the Orthopedic Table Top.
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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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.