NA 11141 (REF 11141-000115)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00883873994429), received between Apr 26, 2021 and Apr 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Electrical Shock” (1 report).

7 other recalls cover devices cleared under the same FDA submission (K142430); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 26, 2021Unintended Electrical Shock; Unintended Electrical Shock

  THE CUSTOMER CONTACTED PHYSIO-CONTROL TO REPORT THAT THEIR DEVICE CHARGING ACCESSORY ELECTROCUTED AND CAUSE ONE OF THEIR EMPLOYEE'S TO BE HOSPITALIZED.

  Patient problems: Electric Shock

  MAUDE report 11725319 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142430. One submission often covers many models, so check the product and lot details in each record.

• Z-0817-2020 · Dec 20, 2019 · Terminated
  LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
• Z-0816-2020 · Dec 20, 2019 · Terminated
  LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
• Z-0862-2019 · Feb 1, 2019 · Terminated
  LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BL
• Z-0863-2019 · Feb 1, 2019 · Terminated
  LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic lif
• Z-1144-2017 · Jan 16, 2017 · Terminated
  LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environ
• Z-1123-2017 · Jan 12, 2017 · Terminated
  LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external de
• Z-1993-2016 · Jan 27, 2016 · Terminated
  LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature installed. Part numbers: V15-2-xxxxxx (includes software version 1 and version 2); V15-5-xxxxxx (inclues soft