FDA Adverse Event Injury Summary report: N

CRAWFORD LACRINAL INTUBATION SET W/SUTURE

MDR report key: 282927 · Received June 22, 2000

Report

Report Number
1926681-2000-00001
Event Type
Injury
Date Received
June 22, 2000
Date of Event
May 17, 2000
Report Date
June 15, 2000
Manufacturer
JEDMED INSTRUMENT CO.
Product Code
HMX
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ATTEMPTED LACRINAL INTUBATION USING CRAWFORD TUBES - LEFT NEEDLE CAME OFF SILICONE TUBING. FURTHER ATTEMPTS TO REINTUBATE FAILED AND FACILITY DISCOVERED THERE IS A SMALL PIECE OF SILICONE LEFT IN PT. PT WILL HAVE TO RETURN AT A LATER DATE FOR "D.C.R."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CRAWFORD LACRINAL INTUBATION SET W/SUTURE LACRINAL INTUBATION TUBING HMX JEDMED INSTRUMENT CO. * *

Patients

Seq Age Sex Outcome Treatment
1 NA Other