Medline FCE1232ABNRecalls & reported problems
Medline Industries, Inc. · BAR,ASSIST,FLIP DOWN FOR FCE1232 BED · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 40884389106427), received between Aug 26, 2020 and Sep 28, 2026 — classified as 2 injuries, 6 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (4 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
- Loose or Intermittent Connection4
- Adverse Event Without Identified Device or Use Problem2
- Fracture1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Laceration(s)2
- Skin Tears1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923845 ↗MalfunctionSep 18, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829613 ↗MalfunctionSep 18, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50821011 ↗MalfunctionSep 16, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794026 ↗MalfunctionSep 11, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50732591 ↗InjuryAug 29, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ACCORDING TO THE CUSTOMER, ON (B)(6) 2025, A RIGHT LOWER LEG "DEGLOVING INJURY" WAS SUSTAINED BY A USER OF THE DEVICE WHILE TRANSFERRING FROM A "WHEELCHAIR TO BED." THE USER HAS BEEN HOSPITALIZED IN ACUTE CARE FOR THE "PAST TWO WEEKS" FOLLOWING SURGERY AND WOUND VAC PLACEMENT.
Patient problems: Skin Tears
MAUDE report 22921043 ↗MalfunctionNov 30, 2020Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED A PATIENT WAS INJURED WHILE WORKING WITH TWO THERAPISTS ON TRANSFERS INTO BED. PATIENT SUSTAINED AN INJURY TO HER LOWER RIGHT LEG THAT REQUIRED MEDICAL ATTENTION.
Patient problems: Laceration(s)
MAUDE report 10920025 ↗InjuryAug 26, 2020Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT EXPERIENCED A BACKWARD FALL AND HIT HER HEAD ON THE ASSIST BAR.
Patient problems: Laceration(s)
MAUDE report 10456106 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page