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

Recall Z-1251-2013 — Mercury Spinal System DIA 5.5 x 80 MM Lordosed Rod, Part Number: 60100-080. Intended to provide immobilization and stabilization of the spine in skeletally mature patients.

U.S. FDA — Device Enforcement · United States · 2009-04-17 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1251-2013
Date of alert
2009-04-17
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Spinal Elements, Inc
Product category
device
Product type
Devices
Reported risk: Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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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