BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE
Report
- Report Number
- 9616656-2019-00112
- Event Type
- Malfunction
- Date Received
- January 28, 2019
- Date of Event
- January 7, 2019
- Report Date
- February 12, 2019
- Manufacturer
- BECTON DICKINSON AND CO.
- Product Code
- FMI
- UDI-DI
- 00382903251056
- PMA / PMN Number
- K131358
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
INVESTIGATION: ONE SEALED 31G X 8MM PEN NEEDLE SAMPLE WAS RETURNED FROM LOT. NO. 8122822, 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 THAT BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE WENT THROUGH OUTER SHIELD AND HAD STERILITY ISSUES. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED, BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.
IT WAS REPORTED THAT BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE WENT THROUGH OUTER SHIELD AND HAD STERILITY ISSUES. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 76133 | BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE | PEN NEEDLE | FMI | BECTON DICKINSON AND CO. | 8122822 | 00382903251056 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |