Sizewise BSWRP2 12060307-120VRecalls & reported problems
Sizewise Rentals, L.L.C. · Bari Rehab Platform2 (80") · Class 2
Data updated Oct 18, 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 00845699003952), received between Jun 4, 2025 and Jun 4, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
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.
MalfunctionJun 4, 2025Use of Device Problem; Use of Device Problem
FACILITY STATES THE RH SIDERAIL BUTTON WOULD NOT ENGAGE IN ORDER TO LET THE SIDERAIL DOWN. 6/4/2025 RECEIVED CONFIRMATION THAT PATIENT WAS ON BEDFRAME AT TIME OF REPORTED ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22146310 ↗
Other Bed, Ac-Powered Adjustable Hospital devices
- Centrella™ Bed P7900BHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL2 recalls5 deaths1,937 reports
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- 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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