MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-09 for CAP TIP SYR LL/LS STER LF PP NAT 50/TRAY 305822 manufactured by Becton Dickinson Medical Systems.
Report Number | 1213809-2019-00908 |
MDR Report Key | 8976079 |
Date Received | 2019-09-09 |
Date of Report | 2019-10-22 |
Date of Event | 2019-08-21 |
Date Mfgr Received | 2019-08-23 |
Device Manufacturer Date | 2018-07-31 |
Date Added to Maude | 2019-09-09 |
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 | 8015652341 |
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 | 3 |
Brand Name | CAP TIP SYR LL/LS STER LF PP NAT 50/TRAY |
Generic Name | LIQUID MEDICATION DISPENSER |
Product Code | KYW |
Date Received | 2019-09-09 |
Catalog Number | 305822 |
Lot Number | 8212539 |
Device Availability | * |
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 | 2019-09-09 |