CATH PKGD: BERMAN 5 FR 8 0CM
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
(B)(4). FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
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 |