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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNKNOWN MEDICAL BED; BED, AC-POWERED ADJUSTABLE HOSPITAL

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UNKNOWN MEDICAL BED; BED, AC-POWERED ADJUSTABLE HOSPITAL Back to Search Results
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 04/21/2024
Event Type  malfunction  
Event Description
The reporter was calling on behalf of a patient who was experiencing a product problem with her medical bed.Reporter stated that the plug that controls the bed broke inside the socket and the bed no longer moves up or down and has lost all function.
 
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Brand Name
MEDICAL BED
Type of Device
BED, AC-POWERED ADJUSTABLE HOSPITAL
Manufacturer (Section D)
UNKNOWN
MDR Report Key19163873
MDR Text Key340964484
Report NumberMW5154092
Device Sequence Number1
Product Code FNL
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 04/22/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received04/22/2024
Patient Sequence Number1
Patient Age100 YR
Patient SexFemale
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