BD INTIMA II¿ IV CATHETER PRN ADAPTER
Report
- Report Number
- 3006948883-2018-00248
- Event Type
- Malfunction
- Date Received
- November 5, 2018
- Date of Event
- October 17, 2018
- Report Date
- November 14, 2018
- Manufacturer
- BD (SUZHOU)
- Product Code
- FOZ
- PMA / PMN Number
- N/A
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- NURSE
Narratives
INVESTIGATION SUMMARY: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 8141365. OUR RECORDS SHOW THE REPORTED LOT WAS MANUFACTURED ON JULY 2018, AND DETERMINED THAT THIS IS THE ONLY INSTANCE OF THIS ISSUE OCCURRING IN THIS PRODUCTION BATCH. ACCORDING TO THE SAMPLING PLAN APPLIED FOR PRODUCT PERFORMANCE, THIS LOT WAS ACCEPTED AND RELEASED WITHOUT DEFECTS BEING NOTED DURING THE FINAL ASSEMBLY OR VISUAL INSPECTIONS OF PACKAGED GOODS. UNFORTUNATELY A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING, WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT.
IT WAS REPORTED WITH THE USE OF THE BD INTIMA II¿ IV CATHETER PRN ADAPTER THERE WAS AN ISSUE WITH SEPARATION DURING USE CAUSING LEAKAGE. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.
IT WAS REPORTED WITH THE USE OF THE BD INTIMA II¿ IV CATHETER PRN ADAPTER THERE WAS AN ISSUE WITH SEPARATION DURING USE CAUSING LEAKAGE. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 876553 | BD INTIMA II¿ IV CATHETER PRN ADAPTER | INTRAVASCULAR CATHETER | FOZ | BD (SUZHOU) | 8141365 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |