INVACARE® BAR600 BARIATRIC BED BAR600IVCRecalls & reported problems
Invacare Corporation · IVC BARIATRIC BED · Class 2
Data updated Oct 18, 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 00841447102687), received between Jan 27, 2025 and Jan 27, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fire” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fire1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 27, 2025Fire; Fire
THE REPORTER STATED THE BAR600IVC BED CAUGHT FIRE. THEY STATED NO INJURIES OR DAMAGES WERE REPORTED. THIS BED WAS IN AN ASSISTED LIVING FACILITY AND WAS CONFIRMED TO BE PLUGGED IN VIA EXTENSION CORD. ACCORDING TO THE FACILITY, THE FIRE WAS NEAR THE JUNCTION BOX OR THE MOTORS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21245641 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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