VersaCare® Med Surg Bed P3201KRecalls & reported problems
Hill-Rom, Inc. · Hospital Bed · Class 2
All models of VersaCare Med Surg Bed (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00887761000889), received between Oct 15, 2024 and Jul 21, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (5 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.
Reports received per month
Most reported problems
Device problems
- Unintended Movement5
- Material Split, Cut or Torn1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 21, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25884903 ↗MalfunctionJul 21, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25884836 ↗MalfunctionMay 27, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT VERSACARE FRAME HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25311547 ↗MalfunctionApr 16, 2026Unintended Movement
IT WAS FOUND THAT THE DEVICE HAD UNRELIABLE BRAKE HOLDING CAPACITY. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24897450 ↗MalfunctionApr 15, 2026Unintended Movement
DURING DEA RESULT IT WAS REPORTED THAT VERSACARE FRAME HAD BRAKES NOT HOLDING WHILE ENGAGED. THIS OCCURRED DURING BAXTER SERVICING./TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24889575 ↗MalfunctionOct 29, 2024Material Split, Cut or Torn; Material Split, Cut or Torn
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20558488 ↗MalfunctionOct 15, 2024Sparking; Sparking
IT WAS REPORTED THAT SPARKS ARE COMING FROM THE NEAR SIDE OF THE HEAD CASTER. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20457493 ↗
Other BED, FLOTATION THERAPY, POWERED devices
- Compella™Bariatric Bed P7800AHill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED1 recall1 death362 reports
- pro+ P7924A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED4 recalls3 reports
- pro+ P7924ARENT01Hill-Rom, Inc. · Bed, Flotation Therapy, Powered3 recalls1 death15 reports
- pro+ P3255A02Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls8 reports
- pro+ P7924A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls4 reports
- pro+ P3255A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls3 reports
- pro+ P7923A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls2 reports
- pro+ P7923A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page