Synergy® Surface P004651Recalls & reported problems
Hill-Rom, Inc. · Hospital Bed Surface · Class 2
All models of Synergy Surface (4)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761016514), received between Oct 15, 2024 and Oct 15, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Frayed” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Frayed1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 15, 2024Material Frayed; Material Split, Cut or Torn; Material Frayed; Material Split, Cut or Torn
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THAT MATTRESS SAE 36"X84" POWER CORD WAS FRAYED WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT AND 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 20454674 ↗
Other Bariatric bed devices
- Medline MDR107004Medline Industries, Inc. · Bariatric bed110 reports
- MV3 5900Stryker Corporation · Bariatric bed1 recall41 reports
- Medline FCEALTMAXXMedline Industries, Inc. · Bariatric bed84 reports
- Synergy® Surface P6881CAPHill-Rom, Inc. · Bariatric bed2 reports
- Drive P503Drive Devilbiss Healthcare · Bariatric bed2 reports
- Joerns Bari10AJoerns Healthcare, LLC · Bariatric Bed2 reports
- Drive 15300BV-PKGDrive Devilbiss Healthcare · Bariatric bed2 reports
- drive PLTCABLDrive Devilbiss Healthcare · Bariatric bed1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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