Freemie FG076Recalls & reported problems
Dao Health · Independence Deluxe Set · 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 00851690007448), received between Jul 18, 2018 and Jul 18, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Smoking” (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
- Smoking1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 18, 2018Smoking; Smoking
ON (B)(6) 2018 - THE CUSTOMER REPORTED HER PUMP STARTED SMOKING. ON (B)(6) 2018 - DURING CUSTOMER SERVICE'S CALL THE CUSTOMER REPORTED "SMOKE CAME FROM THE PUMP PORT, THE PUMP WAS FULLY CHARGED, SHE WAS SITTING ON SOFA WHEN IN USE, AFTER 10 MINUTES THE PUMP STARTED TO SMOKE." THE CUSTOMER ALSO NOTED THAT SHE TOOK PUMP APART TO TRY TO IDENTIFY WHERE THE SMOKE WAS COMING FROM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7701515 ↗
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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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