CONAIR WW711FRecalls & reported problems
Conair Corporation · BMI Scale · Class 2
- 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 00074108337290), received between Aug 10, 2020 and Aug 10, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Explosion” (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
- Explosion1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 10, 2020Explosion
7/6/2020: THE CONSUMER CLAIMS THE PRODUCT EXPLODED. THE CONSUMER ACCEPTED A REPLACEMENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10388145 ↗
Other Analyzer, Body Composition devices
- CONAIR WW702FConair Corporation · Analyzer, Body Composition1 report
- CONAIR WW707YFConair Corporation · Analyzer, Body Composition1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.