Filac 505000Recalls & reported problems
Cardinal Health, Inc. · 3000 AD Electronic Thermometer,Oral/Axillary Complete System with 4 foot (1.2 m) Cord · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521008509), received between Apr 17, 2018 and Apr 17, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Power Problem” (1 report).
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
Device problems
- Power Problem1
- Thermal Decomposition of Device1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 17, 2018Thermal Decomposition of Device; Power Problem; Thermal Decomposition of Device; Power Problem
THE CUSTOMER DID NOT STATE A SPECIFIC ISSUE, BUT SERVICE FOUND THE UNIT DID NOT TURN ON DURING TRIAGE. THE TECHNICIAN FOUND WHAT APPEARS TO BE BURN MARKS ON WHITE CONNECTORS ON PCBA AND BATTERY HOUSING ASSEMBLY.
Patient problems: No Information
MAUDE report 7437935 ↗
Other Thermometer, electronic, clinical devices
- Welch Allyn, Inc. 901054Welch Allyn, Inc. · Thermometer, electronic, clinical1 recall221 reports
- Welch Allyn, Inc. 901054Welch Allyn, Inc. · Thermometer, electronic, clinical2 recalls13 reports
- NA B105 VSP3.0 Patient MonitorGE Medical Systems Information Technologies, Inc. · Thermometer, electronic, clinical2 recalls0 reports
- Medline MDSTH1002Medline Industries, Inc. · Thermometer, electronic, clinical65 reports
- Mon-a-Therm 90050Covidien LP · Thermometer, electronic, clinical1 recall3 reports
- Mon-a-Therm 90044Covidien LP · Thermometer, electronic, clinical1 recall2 reports
- Temperature Probes Esophageal/Rectal Temperature ProbePhilips Medical Systems Hsg · Thermometer, electronic, clinical1 recall1 report
- CARESCAPE B450 MBA313GE Healthcare Finland Oy · Thermometer, electronic, clinical1 recall1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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