FDA Adverse Event Malfunction Summary report: N

CATH PKGD: BERMAN 5 FR 8 0CM

MDR report key: 2043168 · Received February 24, 2011

Report

Report Number
2242445-2011-00025
Event Type
Malfunction
Date Received
February 24, 2011
Date of Event
February 8, 2011
Report Date
February 18, 2011
Manufacturer
ARROW INTL., INC.
Product Code
DQO
PMA / PMN Number
PREAMENDMENT
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED THAT WHILE THE CATHETER WAS IN USE, THE CATHETER BODY BURST UNDER HIGH PRESSURE. AS A RESULT, THE CATHETER WAS REMOVED FROM THE PATIENT (PT) INTACT. THERE WAS NO DELAY IN TREATMENT, NO PT DEATH AND NO PT COMPLICATIONS WERE REPORTED. ADDITIONAL INFORMATION RECEIVED FROM THE HOSPITAL ADMINISTRATIVE ASSISTANT ON (B)(6) 2011 STATED, THEY DO NOT DOCUMENT IN THEIR CASE NOTES, THAT PERCUTANEOUS SHEATH INTRODUCER (PSI) IS USED. THE REPEAT BACK TO THE DOCTOR'S THE VOLUME, FLOW RATE AND PSI PRIOR TO EACH INJECTION AND GET VERIFICATION TO ENSURE SAFETY. RANGES FOR ALL CATHETERS ARE ATTACHED TO THE INJECTOR AND VERIFIED ON EACH CATHETER'S PACKAGE PRIOR TO USE. WHEN THIS FIRST OCCURRED THEY TRIED USING TWO ADDITIONAL KITS WITH THE SAME OUTCOME. AS A RESULT, A SHORTER 5-50 BERMAN WAS USED SUCCESSFULLY FOR THE PT. THE SHAFT THAT BURST WAS OUTSIDE THE PT'S BODY SO THERE WAS NO HARM TO THE PT. REFERENCE MDR #2242445-2011-00026 FOR THE SECOND EVENT AND MDR #2242445-2011-00027 FOR THE THIRD EVENT INVOLVING THE SAME PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CATH PKGD: BERMAN 5 FR 8 0CM BERMAN ANGIOGRAPHIC CATHETER PRODUCTS DQO ARROW INTL., INC. NA

Patients

Seq Age Sex Outcome Treatment
1 4 YR