FDA Adverse Event Malfunction Summary report: N

PROGRESSA FRAME

MDR report key: 11964539 · Received June 9, 2021

Report

Report Number
1824206-2021-00294
Event Type
Malfunction
Date Received
June 9, 2021
Date of Event
June 5, 2021
Report Date
June 5, 2021
Manufacturer
HILL-ROM BATESVILLE
Product Code
FNL
PMA / PMN Number
K122473
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILLROM TECHNICIAN FOUND THE EXTERNAL ALARM NEEDED TO BE REPLACED. PER THE PROGRESSA USER MANUAL: THE BRAKE NOT SET IS AN AUDIBLE AND VISUAL ALARM. THE ALARM WILL SOUND, AND A MESSAGE WILL SHOW ON THE GCI, WHEN THE BED IS CONNECTED TO AN AC POWER SOURCE AND THE BRAKE IS NOT SET. WHEN THE BED IS CONNECTED TO AC POWER AND THE BRAKES ARE NOT SET, AN ALARM SOUNDS AND A MESSAGE SHOWS ON THE GCI. WHEN AC POWER IS REMOVED, THE ALARM WILL STOP AND THE GCI WILL TURN OFF. A SEARCH OF THE HILLROM MAINTENANCE RECORDS DID NOT SHOW HILLROM PERFORMED ANY PREVENTATIVE MAINTENANCE ON THIS BED. IT IS UNKNOWN IF THE FACILITY PERFORMS PREVENTATIVE MAINTENANCE ON THEIR BEDS. THE TECHNICIAN REPLACED THE EXTERNAL ALARM TO RESOLVE THE ISSUE. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

Description of Event or Problem · 1

HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE BED HAD NO AUDIBLE BRAKE NOT SET ALARM. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
863261 PROGRESSA FRAME BED, AC-POWERED ADJUSTABLE HOSPITAL FNL HILL-ROM BATESVILLE P7500A000131

Patients

Seq Age Sex Outcome Treatment
1