BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE
Report
- Report Number
- 9616656-2019-00103
- Event Type
- Malfunction
- Date Received
- January 25, 2019
- Date of Event
- January 8, 2019
- Report Date
- February 12, 2019
- Manufacturer
- BECTON DICKINSON AND CO.
- Product Code
- FMI
- PMA / PMN Number
- K131358
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
H.6. INVESTIGATION: ONE OPEN 31G X 8MM PEN NEEDLE SAMPLE WAS RETURNED FROM LOT. NO. 8143587, CAT. NO. 325105. VISUAL EXAMINATION WAS CARRIED OUT ON THE RETURNED SAMPLE AND A CANNULA THROUGH SHIELD AND COVER WAS OBSERVED. A LOT HISTORY REVIEW WAS CARRIED OUT AND NO RELATED NON CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS PACKAGED LOT CONCLUDING ALL INSPECTIONS WERE PERFORMED PER THE APPLICABLE OPERATIONS AND MET QC SPECIFICATIONS. ROOT CAUSE OF THIS ISSUE WAS INCORRECT LOADING OF THE SHIELD TO THE HUB AT THE SHIELDING STATION.
IT WAS REPORTED WITH THE USE OF THE BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE THERE WAS AN ISSUE WITH NEEDLE THROUGH THE PROTECTIVE COVER UPON OPENING THE PACKAGING.
(B)(6). 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 MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE THERE WAS AN ISSUE WITH NEEDLE THROUGH THE PROTECTIVE COVER UPON OPENING THE PACKAGING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 69699 | BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE | PEN NEEDLE | FMI | BECTON DICKINSON AND CO. | 8143587 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |