MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-29 for BARREL 10CC LL W/SILICONE NO BD LOGO BNS 304157 manufactured by Becton Dickinson Medical Systems.
[134579398]
Date of event: unknown. The date received by manufacturer has been used for this field. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10
[134579399]
It was reported that 10,285 syringe barrels 10cc ll w/silicone no bd logo bns exhibited "pools/droplets" of excess silicone in them once the plunger was inserted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1213809-2019-00126 |
MDR Report Key | 8287274 |
Date Received | 2019-01-29 |
Date of Report | 2019-04-11 |
Date of Event | 2019-01-09 |
Date Mfgr Received | 2019-01-09 |
Device Manufacturer Date | 2018-04-27 |
Date Added to Maude | 2019-01-29 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | BDX BRETT WILKO |
Manufacturer Street | 9450 SOUTH STATE STREET |
Manufacturer City | SANDY UT 84070 |
Manufacturer Country | US |
Manufacturer Postal | 84070 |
Manufacturer Phone | 8015652845 |
Manufacturer G1 | BECTON DICKINSON MEDICAL SYSTEMS |
Manufacturer Street | ROUTE 7 AND GRACE WAY |
Manufacturer City | CANAAN CT 06018 |
Manufacturer Country | US |
Manufacturer Postal Code | 06018 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | BARREL 10CC LL W/SILICONE NO BD LOGO BNS |
Generic Name | SYRINGE BARREL |
Product Code | KDC |
Date Received | 2019-01-29 |
Returned To Mfg | 2019-01-16 |
Catalog Number | 304157 |
Lot Number | 8117555 |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON DICKINSON MEDICAL SYSTEMS |
Manufacturer Address | ROUTE 7 AND GRACE WAY CANAAN CT 06018 US 06018 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-01-29 |