MedSurg Manual Bed FL23PRecalls & reported problems
Umano Medical Inc · MedSurg Manual Bed · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00670482000029), received between Jul 17, 2018 and Jul 29, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Mechanical Problem4
Patient problems
- No Patient Involvement4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 29, 2019Mechanical Problem; Mechanical Problem
THIS REPORT SUMMARIZES <NOE> 4 </NOE> MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE UNIT HAD REDUCED BRAKE FORCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 8836109 ↗MalfunctionJan 25, 2019Mechanical Problem; Mechanical Problem
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE UNIT HAD REDUCED BRAKE FORCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 8279231 ↗MalfunctionOct 26, 2018Mechanical Problem; Mechanical Problem
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE UNITS HAD REDUCED BRAKE FORCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 8009848 ↗MalfunctionJul 17, 2018Mechanical Problem; Mechanical Problem
THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE UNITS HAD REDUCED BRAKE FORCE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 7693549 ↗
Other Bed, Manual devices
- Drive 15201BVDrive Devilbiss Healthcare · BED, MANUAL2 deaths5 reports
- Drive 15021BVDrive Devilbiss Healthcare · BED, MANUAL2 reports
- Drive 16500BVDrive Devilbiss Healthcare · BED, MANUAL1 report
- SleepSafe Manual Hi-Lo ComboSleepsafe Beds, LLC · Bed, Manual1 report
- Drive 1222PDrive Devilbiss Healthcare · BED, MANUAL1 death1 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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page