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

Recall Z-2545-2015 — MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC

U.S. FDA — Device Enforcement · United States · 2015-08-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2545-2015
Date of alert
2015-08-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Covidien LLC
Product category
device
Product type
Devices
Reported risk: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns
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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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.