ook snow ALL 200-0000 (UDI 00670482000142)Recalls & reported problems
Umano Medical Inc · AC-powered medical bed with 4 built-in electric DC actuators that offers a powered adjustment of the height and surface contours. Bed includes movable and latchable siderails, and control boards. The patient sleep surface can be manually extended of 4” with the integrated bed length extender and reach 84” or 88” long. The surface width can be manually extended from 35” up to 47”. The product offers a range of options and accessories including but not limited to integrated scale, integrated bed exit system, fixed or foldable IV pole, patient helper, oxygen bottle holder and length extension cushions. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00670482000142), received between Jun 26, 2020 and Mar 5, 2024 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Defective Component” (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
- Defective Component1
- Detachment of Device or Device Component1
- Electrical /Electronic Property Problem1
- Mechanical Problem1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Bone Fracture(s)1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 5, 2024Mechanical Problem; Mechanical Problem
CUSTOMER REPORTED TO THE TECHNICAL SERVICE OF MANUFACTURER THAT BOTH BREAKING/STEER BAR ASSEMBLIES OF THE BED WERE COMPLETELY RIPPED OFF. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18839779 ↗MalfunctionMar 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
CUSTOMER CALLED THE TECHNICAL SERVICE OF MANUFACTURER TO REPORT ABOUT A BED WITH TWO BROKEN BRAKING BARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18839381 ↗MalfunctionNov 24, 2022Defective Component; Defective Component
THE MANUFACTURER WAS INFORMED THAT THE BRAKING SYSTEM OF THE BED IS BROKEN. THE CUSTOMER MENTIONED THAT THE BRAKING BAR WAS AFFECTED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15860930 ↗MalfunctionMay 19, 2021Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
IT WAS REPORTED THAT THE BED WOULD NOT GIVE AUDIBLE SIGNAL ON THE BED EXIT DETECTION. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11852233 ↗InjuryJun 26, 2020Use of Device Problem; Use of Device Problem
TECHNICAL SERVICE DEPARTMENT OF THE MANUFACTURER WAS CONTACTED BY CLIENT REPORTING THAT A "RN WALKED INTO ROOM AT APPROXIMATELY 2AM AND FOUND PATIENT ON THE GROUND KNEELING NEXT TO THE BED. BED EXIT ALARMS WAS NOT SET BECAUSE RN STATED THAT SHE "DIDN'T KNOW HOW". UNKNOWN IF PATIENT FELT." IT WAS FURTHER REPORTED THAT PATIENT RE-BROKE THEIR PELVIS.
Patient problems: Bone Fracture(s)
MAUDE report 10203274 ↗
Other Bed, Ac-Powered Adjustable Hospital devices
- Centrella™ Bed P7900BHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL2 recalls5 deaths1,937 reports
- Progressa® Bed System P7500AHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death1,377 reports
- VersaCare® Med Surg Bed P3200KHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL3 deaths1,193 reports
- Medline MDR107002EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death374 reports
- Medline MDR107003EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall3 deaths362 reports
- InTouch 2141Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths361 reports
- Citadel Plus FX811B3B4AMABBArjohuntleigh AB · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths358 reports
- TotalCare® Bed P1900QHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL317 reports
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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