FDA Adverse Event Injury Summary report: N

STARTER KIT, SIZE 4, 1214

MDR report key: 94671 · Received May 27, 1997

Report

Report Number
1224675-1997-00034
Event Type
Injury
Date Received
May 27, 1997
Date of Event
May 12, 1997
Report Date
May 15, 1997
Manufacturer
UROMED CORP.
Product Code
MNG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT REPORTED SHE COULD NOT FIND DEVICE WHEN SHE PULLED THE STRING. DEVICE WAS LATER FOUND ON FLOOR AND HAD NOT MIGRATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 STARTER KIT, SIZE 4, 1214 RELIANCE MNG UROMED CORP. SIZE 4 0000000009

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention