LUCAS CHEST COMPRESSION SYSTEM 11576Recalls & reported problems
Jolife AB · LUCAS BATTERY DARK GRAY · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00883873861820), received between Dec 15, 2023 and Jan 2, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fire” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Fire2
- Electrical /Electronic Property Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 2, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
THE CUSTOMER CONTACTED STRYKER TO REPORT THAT THEIR DEVICE'S BATTERY BATTERY CAUGHT FIRE. THIS MAY LEAD TO INJURY AS A RESULT OF THE FIRE. THERE WAS NO PATIENT INVOLVEMENT REPORTED DURING THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18430024 ↗MalfunctionDec 15, 2023Fire; Fire
THE CUSTOMER CONTACTED STRYKER TO REPORT A BATTERY FOR ONE OF THEIR DEVICES CAUGHT FIRE. THE CUSTOMER ADVISED THEY WERE PERFORMING A ROUTINE CHECK ON THEIR EQUIPMENT AND NOTICED SMOKE EMITTING FROM A BATTERY THAT WAS IN ITS CHARGER. THE CUSTOMER REMOVED THE BATTERY FROM THE CHARGER AND PLACED IT ON THE BAY FLOOR. THE BATTERY THEN CAUGHT ON FIRE AND ENGULFED THE BATTERY. THE BATTERY IS USED FOR AN AUTOMATED CHEST COMPRESSION DEVICE. THERE WAS NO PATIENT USE ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18335223 ↗MalfunctionDec 15, 2023Fire; Fire
THE CUSTOMER CONTACTED STRYKER TO REPORT A BATTERY FOR ONE OF THEIR DEVICES CAUGHT FIRE. THE CUSTOMER ADVISED THEY WERE PERFORMING A ROUTINE CHECK ON THEIR EQUIPMENT AND NOTICED SMOKE EMITTING FROM A BATTERY THAT WAS IN ITS CHARGER. THE CUSTOMER REMOVED THE BATTERY FROM THE CHARGER AND PLACED IT ON THE BAY FLOOR. THE BATTERY THEN CAUGHT ON FIRE AND ENGULFED THE BATTERY. THE BATTERY IS USED FOR AN AUTOMATED CHEST COMPRESSION DEVICE. THERE WAS NO PATIENT USE ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18335220 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.