VersaCare Med Surg BedRecalls & reported problems across all models
Hill-Rom, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,200
- Deaths reported
- 3
- Injuries reported
- 3
- Recalls
- 0
We found 2 models of VersaCare Med Surg Bed by Hill-Rom, Inc. in the FDA's device registry (GUDID). Together they are named in 1,200 adverse event reports in the FDA's MAUDE database, received between Feb 4, 2021 and Sep 22, 2026 — classified as 3 deaths, 3 injuries, 1,194 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (710 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported VersaCare Med Surg Bed problems
Device problems
- Material Split, Cut or Torn710
- Unintended Movement366
- No Audible Alarm56
- Defective Alarm28
- Activation Problem14
- Material Frayed10
- Sparking5
- Collapse4
Patient problems
- No Clinical Signs, Symptoms or Conditions1,189
- Fall4
- No Consequences Or Impact To Patient3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bone Cement Implantation Syndrome1
- Bone Fracture(s)1
- Hip Fracture1
- Insufficient Information1
VersaCare Med Surg Bed models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- VersaCare® Med Surg Bed P3200KBED, AC-POWERED ADJUSTABLE HOSPITAL3 deaths1,193 reports
- VersaCare® Med Surg Bed P3201KBED, FLOTATION THERAPY, POWERED7 reports
Recent VersaCare Med Surg Bed adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50862550 ↗MalfunctionSep 18, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831369 ↗MalfunctionSep 18, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831335 ↗MalfunctionSep 18, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831210 ↗MalfunctionSep 17, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810182 ↗MalfunctionSep 17, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50797054 ↗MalfunctionSep 16, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50796480 ↗MalfunctionSep 16, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795843 ↗MalfunctionSep 16, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793184 ↗MalfunctionSep 15, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781878 ↗MalfunctionSep 15, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781847 ↗MalfunctionSep 15, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781772 ↗MalfunctionSep 15, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781437 ↗MalfunctionSep 15, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777486 ↗MalfunctionSep 15, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776605 ↗
Other Hill-Rom, Inc. products
- Centrella Bed2 models · 2,021 reports · 2 recalls
- pro+18 models · 36 reports · 13 recalls
- Voalte Nurse Call2 models · 419 reports · 2 recalls
- ALLEN24 models · 73 reports · 5 recalls
- WatchCare4 models · 0 reports · 4 recalls
- NaviCare Nurse Call Systems3 models · 99 reports · 2 recalls
- CompellaSurface3 models · 87 reports · 1 recall
- Progressa Surface13 models · 8 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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