FDA Adverse Event Malfunction Summary report: N

FASTLOAD CTA DUAL SYRINGE PACK

MDR report key: 20074979 · Received August 27, 2024

Report

Report Number
20074979
Event Type
Malfunction
Date Received
August 27, 2024
Date of Event
August 21, 2024
Report Date
August 23, 2024
Manufacturer
BRACCO INJENEERING S.A.
Product Code
DXT
UDI-DI
17630039300880
Product Problem
Yes
Report Source
User Facility report
Reporter Location
OH
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

PROCEDURE: CT, NEW BRACCO- FASTLOAD CTA DUAL SYRINGE PACK OPENED- MISSING THE TUBING. NOT USED ON PATIENT. MANUFACTURER RESPONSE FOR INJECTOR AND SYRINGE, ANGIOGRAPHIC, FASTLOAD CTA DUAL SYRINGE PACK (PER SITE REPORTER). WILL OBTAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
968245 FASTLOAD CTA DUAL SYRINGE PACK INJECTOR AND SYRINGE, ANGIOGRAPHIC DXT BRACCO INJENEERING S.A. 017354 256819 17630039300880

Patients

Seq Age Sex Outcome Treatment
1 NA Prefer Not To Disclose