PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP
Report
- Report Number
- 9615050-2013-00452
- Event Type
- Malfunction
- Date Received
- March 21, 2013
- Date of Event
- January 1, 2012
- Report Date
- February 22, 2013
- Manufacturer
- HOSPIRA COSTA RICA LTD.
- Product Code
- FRN
- PMA / PMN Number
- K982159
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- OTHER
Narratives
THE CUSTOMER CONTACT INDICATED THAT THE DEVICES WERE DISCARDED. INVESTIGATION IS NOT COMPLETE. THIS REPORT REPRESENTS ALL THE INFORMATION KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.
GENERAL REPORT RECEIVED OF AN UNSPECIFIED NUMBER OF UNDOCUMENTED INCIDENTS OF LEAKS. ON UNSPECIFIED DATES, THE OPTION-LOK MALE ADAPTER OF THE TUBING SETS WERE CONNECTED TO THE PT'S IV ACCESS SITES AND WERE BEING USED TO DELIVER EITHER UNSPECIFIED MEDICATIONS OR UNSPECIFIED CHEMOTHERAPEUTIC AGENTS, AT UNSPECIFIED RATES, VIA PLUM PUMPS. AFTER UNSPECIFIED LENGTHS OF TIME, THE CUSTOMER CONTACT REPORTED THAT UNSPECIFIED VOLUMES OF SOLUTIONS LEAKED FROM UNSPECIFIED LOCATIONS AT THE CLAVE SECONDARY PORT ON THE CASSETTE OF THE TUBING SETS ONTO THE PTS AND ONTO THE FLOOR. THE TUBING SETS WERE REPLACED AND THE THERAPIES WERE RESUMED. THERE WERE NO REPORTED ADVERSE PT EFFECTS AND NO REPORTED DELAYS OF THERAPIES CRITICAL TO THESE PTS. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED, INCLUDING IF THE LEAD OF SOLUTIONS WERE CLEANED UP ACCORDING TO THE USER FACILITY'S PROTOCOL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 118985 | PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP | 80FRN | FRN | HOSPIRA COSTA RICA LTD. | NA | 230065H |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |