VersaCare® Med Surg Bed P3200KRecalls & 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
Quick summary
This Hill-Rom VersaCare Med Surg bed is an adjustable hospital bed. Many of its 1,179 reports describe material that splits, tears or frays, and others describe unintended movement and alarms that do not sound. Recent reports mention power cords with exposed copper wires. The reports include 3 deaths and 4 injuries. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 1,193
- Deaths reported
- 3
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,193 adverse event reports that list this exact device (DI 00887761000872), received between Feb 4, 2021 and Sep 22, 2026 — classified as 3 deaths, 3 injuries, 1,187 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (709 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
- Material Split, Cut or Torn709
- Unintended Movement361
- No Audible Alarm56
- Defective Alarm28
- Activation Problem14
- Material Frayed10
- Collapse4
- Sparking4
Patient problems
- No Clinical Signs, Symptoms or Conditions1,182
- 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
Recent adverse event reports
The 25 most recent of 1,193 reports, 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 ↗MalfunctionSep 11, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744341 ↗MalfunctionSep 11, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744277 ↗MalfunctionSep 10, 2026Unintended Movement
Baxter received a report that VERSACARE FRAME had brakes not holding while in brake position. The process step during which this occurred was unknown. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50713667 ↗MalfunctionSep 9, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50702611 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50696052 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695880 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695065 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50694836 ↗MalfunctionSep 8, 2026Unintended System Motion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50679865 ↗MalfunctionSep 8, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674123 ↗
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
- 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
- S3 3005Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall2 deaths242 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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