FDA Adverse Event Injury Summary report: N

MILTEX

MDR report key: 163250 · Received April 15, 1998

Report

Report Number
163250
Event Type
Injury
Date Received
April 15, 1998
Date of Event
February 19, 1998
Report Date
March 31, 1998
Manufacturer
MILTEX INSTRUMENT CO.
Product Code
HRR
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
CO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

NURSE TRIMMING TAPE HOLDING AN ORAL GASTRIC TUBE IN PLACE CUT EAR OF BABY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MILTEX SHEARS HRR MILTEX INSTRUMENT CO. THERE WERE NO IDENTIFYING IMPRINTED ON HANDLE.

Patients

Seq Age Sex Outcome Treatment
1 1 MO Required Intervention REPAIR OF EARLOBE BY PLASTIC SURGEON.