BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE
Report
- Report Number
- 3009081593-2018-00070
- Event Type
- Malfunction
- Date Received
- October 24, 2018
- Date of Event
- October 4, 2018
- Report Date
- November 7, 2018
- Manufacturer
- BECTON DICKINSON HUNGARY KFT (BD)
- Product Code
- MEG
- PMA / PMN Number
- SEE H.10
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SZ
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
NEITHER SAMPLE NOR PHOTO WAS PROVIDED TO BD MEDICAL ¿ PHARMACEUTICAL SYSTEM (BDM-PS) FOR ANALYSIS. BDM-PS PERFORMED A BATCH HISTORY RECORD¿S REVIEW (BHR) INCLUDING A REVIEW OF ALL DATA COLLECTED DURING IN PROCESS AND QUALITY INSPECTIONS. THE BATCHES INVOLVED IN THIS COMPLAINT MEET ALL ACCEPTABLE QUALITY LEVELS (AQL¿S), WERE MANUFACTURED AND RELEASED ACCORDING TO APPLICABLE PROCEDURES AND SPECIFICATIONS. BASED ON INVESTIGATION CONCLUSION, BDM-PS WAS NOT ABLE TO CONFIRM THE SYMPTOM PERCEIVED BY CUSTOMER OR CORRELATE THIS SYMPTOM WITH A POTENTIAL CAUSE LINKED TO BD PROCESS.
IT WAS REPORTED THAT BD ULTRASAFE PASSIVE X-SERIES NEEDLE GUARD SYRINGE LEAKED. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. PMA/510(K)#: K011369, K122558. 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 ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE LEAKED. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 842023 | BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE | PISTON SYRINGE | MEG | BECTON DICKINSON HUNGARY KFT (BD) | 7114347 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |