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

Recall Z-0816-2020 — LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.

U.S. FDA — Device Enforcement · United States · 2019-12-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0816-2020
Date of alert
2019-12-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Physio-Control, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
37964613
Reported risk: Monitor/Defibrillator may not deliver a shock after the "Shock" button on the keypad is pressed as a result of oxidation that has formed over time within the button.
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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