FDA Adverse Event Injury Summary report: N

DBD-WHEELCHAIR, VINYL, DLR, S/A, K2B, 18

MDR report key: 22055360 · Received May 20, 2025

Report

Report Number
1417592-2025-00237
Event Type
Injury
Date Received
May 20, 2025
Date of Event
March 25, 2025
Report Date
May 20, 2025
Manufacturer
MEDLINE INDUSTRIES LP
Product Code
IOR
UDI-DI
00884389830041
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

IT WAS REPORTED THAT "WHEN SHE WAS ASSISTED TO BE PLACED ON WHEELCHAIR HER FEET SLID AND WHEELCHAIR WENT BACK. IT DID NOT STAY IN PLACE. SHE FELL DOWN AND FRACTURED HER HIP." DUE TO THIS, SURGERY AND THERAPY WAS REQUIRED. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT CAUSED OR CONTRIBUTED TO SERIOUS INJURY, THEREFORE, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

Description of Event or Problem · 0

WHEELCHAIR NOT LOCKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
9597 DBD-WHEELCHAIR, VINYL, DLR, S/A, K2B, 18 IOR MEDLINE INDUSTRIES LP 00884389830041

Patients

Seq Age Sex Outcome Treatment
1 80 YR Female Other