FDA Adverse Event Malfunction Summary report: N

9684

MDR report key: 193516 · Received October 22, 1998

Report

Report Number
2183897-1998-00004
Event Type
Malfunction
Date Received
October 22, 1998
Report Date
October 21, 1998
Manufacturer
CROW RIVER INDUSTRIES, INC.
Product Code
ING
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

REPORT OF ALLEGED "PT INJURED WHILE USING A CROW RIVER LIFT." PT ALLEGEDLY FELL OFF HIS LIFT, AND SUSTAINED INJURIES TO THE FACE AND SHOULDER. PT ALLEGES THAT THE PLATFORM TILTED DOWN WHICH CAUSED THE WHEELCHAIR AND HIMSELF TO ROLL OFF AND FALL TO THE GROUND. PT DID HAVE X-RAYS AFTER THE ACCIDENT, BUT DID NOT RECEIVE ANY BROKEN BONES. HE HAS NOT BEEN BACK TO THE DR SINCE THE INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 9684 AUTOMATIC VAN LIFT ING CROW RIVER INDUSTRIES, INC. 9684 NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other