FDA Adverse Event Other Summary report: N

QUIK ABG KIT

MDR report key: 258164 · Received January 4, 2000

Report

Report Number
1718887-1999-00004
Event Type
Other
Date Received
January 4, 2000
Manufacturer
MARQUEST MEDICAL PRODUCTS
Product Code
CBT
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
RESPIRATORY THERAPIST

Narratives

Description of Event or Problem · 1

FOLLOWING THE ACQUISITION OF THE BLOOD SAMPLE THE CLINICIAN INSERTED THE NEEDLE INTO THE GEL-FILLED SHEATH. WHEN THE PROCEDURE WAS COMPLETE, THE CLINICIAN REACHED TO PICK UP THE SYRINGE AND THE GEL-FILLED SHEATH CAME OFF RESULTING IN A NEEDLESTICK TO THEIR FINGER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUIK ABG KIT ARTERIAL BLOOD GAS SAMPLING SYRINGE CBT MARQUEST MEDICAL PRODUCTS NA UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other