FDA Adverse Event Malfunction Summary report: N

HI-TORQUE WHISPER GUIDE WIRES

MDR report key: 18144789 · Received November 15, 2023

Report

Report Number
2024168-2023-12737
Event Type
Malfunction
Date Received
November 15, 2023
Date of Event
October 1, 2023
Report Date
November 15, 2023
Manufacturer
ABBOTT VASCULAR
Product Code
DQX
UDI-DI
08717648116094
PMA / PMN Number
K101116
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
BR
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE PRODUCT WAS NOT RETURNED TO ABBOTT VASCULAR FOR ANALYSIS. A REVIEW OF THE ELECTRONIC LOT HISTORY RECORD (ELHR), CORRECTIVE ACTION TRACKING SYSTEM FOR THE WEB (CATSWEB) DATABASE REVIEW, AND SIMILAR INCIDENT QUERY WERE NOT PERFORMED BECAUSE THE LOT NUMBER WAS NOT PROVIDED. THE INVESTIGATION WAS UNABLE TO DETERMINE A CONCLUSIVE CAUSE FOR THE REPORTED DIFFICULT TO ADVANCE/REMOVE. THERE IS NO INDICATION OF A PRODUCT QUALITY ISSUE WITH RESPECT TO MANUFACTURE, DESIGN, OR LABELING. THE ADDITIONAL GUIDE WIRES REFERENCED IN B5 ARE FILED UNDER SEPARATE MEDWATCH REPORT NUMBERS.

Description of Event or Problem · 0

IT WAS REPORTED IN A GENERAL COMMENT THAT DURING PROCEDURES OF GREATER COMPLEXITY, THE BALANCE MIDDLEWEIGHT (BMW), BMW UNIVERSAL II, BALANCE HEAVYWEIGHT, WHISPER MS AND WHISPER EXTRA SUPPORT GUIDE WIRES LOSE THEIR HYDROPHILICITY. THERE IS RESISTANCE WITH BALLOONS, STENTS AND IMAGING CATHETERS AND THE GUIDE WIRES ARE SIMPLY REMOVED WITH THE OTHER DEVICE AS A SINGLE UNIT BECAUSE THE DEVICES ARE STUCK TO EACH OTHER. THERE WERE NO ADVERSE PATIENT EFFECTS AND THE LENGTH OF THE PROCEDURE IS EXTENDED AND THERE IS GREATER EXPOSURE TO X RAYS BUT THERE IS NO CONSEQUENCE TO THE PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
193754 HI-TORQUE WHISPER GUIDE WIRES GUIDE WIRE DQX ABBOTT VASCULAR 08717648116094

Patients

Seq Age Sex Outcome Treatment
1 Unknown