FDA Adverse Event Injury Summary report: N

MEMBRANE PEELING FORCEPS

MDR report key: 21229 · Received April 18, 1995

Report

Report Number
MW1005646
Event Type
Injury
Date Received
April 18, 1995
Date of Event
January 5, 1995
Report Date
March 19, 1995
Manufacturer
GRIESHABER & CO., INC.
Product Code
HNR
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

SCISSORS MALFUNCTIONED AND 1 OF THE BLADES DROPPED OUT OF THE UNIT AND FELL TO THE RETINAL SURFACE. REMOVED THROUGH ENLARGED SCLEROTOMY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEMBRANE PEELING FORCEPS MEMBRANE PEELING FORCEPS HNR GRIESHABER & CO., INC. 1299

Patients

Seq Age Sex Outcome Treatment
1 71 YR Required Intervention