Medline MDS89694NRecalls & reported problems
Medline Industries, Inc. · RAIL,SIDE,SPRING LOADED,4 BAR,1 PAIR · Class 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 40884389118727), received between Apr 23, 2026 and Sep 29, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Mechanical Jam” (3 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
- Mechanical Jam3
- Collapse2
- Fracture2
- Material Integrity Problem2
- Material Separation2
- Material Twisted/Bent2
- Structural Problem2
- Activation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Fall2
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934741 ↗MalfunctionSep 25, 2026Mechanical Jam; Activation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50906165 ↗MalfunctionSep 25, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50904090 ↗MalfunctionSep 24, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885792 ↗MalfunctionAug 12, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50220801 ↗MalfunctionApr 24, 2026Collapse; Material Separation; Structural Problem; Material Integrity Problem; Mechanical Jam
ACCORDING TO THE CUSTOMER, THE SIDE RAIL ON THE BED COLLAPSED IN THE MIDDLE AND THE BLACK SPACERS IN THE MIDDLE CAME OFF. IT WAS ALSO REPORTED THAT THE HEAD REST DOES NOT GO UP OR DOWN AND THERE ARE CABLES STICKING OUT.
Patient problems: Fall
MAUDE report 24984356 ↗MalfunctionApr 23, 2026Collapse; Material Separation; Structural Problem; Material Integrity Problem; Mechanical Jam
ACCORDING TO THE CUSTOMER, THE SIDE RAIL ON THE BED COLLAPSED IN THE MIDDLE AND THE BLACK SPACERS IN THE MIDDLE CAME OFF. IT WAS ALSO REPORTED THAT THE HEAD REST DOES NOT GO DOWN AND THERE ARE CABLES STICKING OUT.
Patient problems: Fall
MAUDE report 24973776 ↗
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
- 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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