MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-01-14 for BD SPINAL NEEDLE 27GA 3-1/2IN 408381 manufactured by Becton Dickinson Industrias Cirurgicas, Ltda..
Report Number | 9610048-2019-00368 |
MDR Report Key | 9587279 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
Date Received | 2020-01-14 |
Date of Report | 2020-03-26 |
Date of Event | 2019-12-11 |
Date Mfgr Received | 2019-12-27 |
Device Manufacturer Date | 2019-03-15 |
Date Added to Maude | 2020-01-14 |
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 INDUSTRIAS CIRURGICAS, LTDA. |
Manufacturer Street | AVE. PRES.JUSCELINO KUBITSCHEK 273 FRANCISCO BERNARDINO |
Manufacturer City | JUIZ DE FORA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BD SPINAL NEEDLE 27GA 3-1/2IN |
Generic Name | SPINAL NEEDLE |
Product Code | MIA |
Date Received | 2020-01-14 |
Catalog Number | 408381 |
Lot Number | 9058939 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA. |
Manufacturer Address | AVE. PRES.JUSCELINO KUBITSCHEK 273 FRANCISCO BERNARDINO JUIZ DE FORA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-01-14 |