IVT DISPOSABLE
Report
- Report Number
- 1416980-2013-01373
- Event Type
- Malfunction
- Date Received
- January 18, 2013
- Date of Event
- December 25, 2012
- Report Date
- December 26, 2012
- Manufacturer
- BAXTER HEALTHCARE - AIBONITO
- Product Code
- KPE
- PMA / PMN Number
- K090096
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TW
- Reporter Occupation
- PHARMACIST
Narratives
(B)(4). ADDITIONAL INFORMATION: ONE UNUSED SAMPLE WAS AVAILABLE FOR EVALUATION. A VISUAL INSPECTION WAS PERFORMED AND PARTICULATE MATTER WAS DISCOVERED INSIDE THE ALL IN ONE BAG. THE REPORTED CONDITION WAS CONFIRMED. NO OTHER TESTS WERE PERFORMED. THE ASSIGNABLE ROOT CAUSE FOR THE REPORTED CONDITION IS UNKNOWN. THIS ISSUE IS BEING INVESTIGATED THROUGH CAPA. SHOULD ADDITIONAL RELEVANT INFORMATION BE RECEIVED, A FOLLOW-UP MEDWATCH WILL BE SUBMITTED.
(B)(4). THE SAMPLE WAS RECEIVED FOR EVALUATION; HOWEVER, THE EVALUATION HAS NOT YET BEEN COMPLETED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF EVALUATION OR IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
(B)(4).INITIAL EVALUATION CONFIRMED THE REPORTED CONDITION. A BATCH REVIEW WAS CONDUCTED AND THERE WERE NO DEVIATIONS FOUND RELATED TO THIS REPORTED CONDITION DURING THE MANUFACTURE OF THIS LOT. UPON COMPLETION OF BAXTER'S INVESTIGATION, A FOLLOW-UP WILL BE SUBMITTED.
THE PHARMACIST OF A FACILITY REPORTED TO BAXTER (B)(4) THAT AN ALL-IN-ONE EMPTY CONTAINER, WITH CONNECTOR (1000ML), WAS FOUND TO HAVE PARTICLES INSIDE IT. THIS WAS OBSERVED BY THE PHARMACIST, PRIOR TO PATIENT USE. THERE IS NO REPORT OF PATIENT INVOLVEMENT, INJURY/ADVERSE EVENTS, OR MEDICAL INTERVENTION IN ASSOCIATION WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 28197 | IVT DISPOSABLE | SET, I.V. FLUID TRANSFER | KPE | BAXTER HEALTHCARE - AIBONITO | UR12H21047 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |