LS CLAVE PORT EXT 7"
Report
- Report Number
- 9615050-2008-00273
- Event Type
- Malfunction
- Date Received
- September 15, 2008
- Date of Event
- January 1, 2008
- Report Date
- August 25, 2008
- Manufacturer
- HOSPIRA HOLDINGS DE COSTA RICA LTD.
- Product Code
- FPA
- PMA / PMN Number
- K915571
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- RADIOLOGIC TECHNOLOGIST
Narratives
THE SAMPLE WAS NOT RETURNED SINCE THIS IS A KNOWN ISSUE. THE ISSUE OF SPLIT OR BURST TUBING WHEN USING POWER INJECTORS WAS EVALUATED UNDER A FORMAL INVESTIGATION. IT WAS DETERMINED THAT THIS IS NOT A MANUFACTURING OR MATERIALS DEFECT. IT WAS COMMUNICATED TO THE CUSTOMER THAT STANDARD I.V. ADMINISTRATION SETS ARE INTENDED FOR GENERAL INFUSION AND NOT RECOMMENDED FOR USE WITH POWER INJECTORS. IN ADDITION, THE INFUSION THERAPY ACCOUNT MANAGERS WERE ADVISED OF THIS ISSUE AND WERE PROVIDED WITH A PRODUCT LIST OF THOSE HIGH-PRESSURE SETS THAT ARE APPROPRIATE FOR USE WITH THE POWER INJECTORS.
THE CUSTOMER CONTACT REPORTED A TUBING RUPTURE WHILE IN USE WITH A POWER INJECTOR; SUBSEQUENTLY, BLOOD LOSS WAS NOTED. THE TUBING SET WAS CONNECTED TO A POWER INJECTOR AND WAS BEING USED TO DELIVER AN UNSPECIFIED CONTRAST MEDIA AT A RATE OF 4ML/SEC TO 5ML/SEC. AFTER AN UNSPECIFIED LENGTH OF TIME IN USE, THE TUBING RUPTURED AT AN UNSPECIFIED LOCATION. THE CUSTOMER CONTACT REPORTED AN UNSPECIFIED VOLUME OF BLOOD WAS LOST. THE TUBING SET WAS REPLACED AND THE PROCEDURE WAS COMPLETED. THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFO WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LS CLAVE PORT EXT 7" | 80-FPA | FPA | HOSPIRA HOLDINGS DE COSTA RICA LTD. | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | UNSPECIFIED POWER INJECTOR |