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

Recall Z-1178-2018 — MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL¿ Connector, REF/Catalog Number 2602Z Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes provide the conductive interfac

U.S. FDA — Device Enforcement · United States · 2018-02-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1178-2018
Date of alert
2018-02-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ConMed Corporation
Product category
device
Product type
Devices
Reported risk: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause 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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