MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2020-02-06 for BD NEEDLE 18X1-1/2 BLUNT FILL 305180 manufactured by Bd Medical (bd West) Medical Surgical.
Report Number | 1911916-2020-00100 |
MDR Report Key | 9678190 |
Report Source | COMPANY REPRESENTATIVE,OTHER |
Date Received | 2020-02-06 |
Date of Report | 2020-01-28 |
Date of Event | 2020-01-23 |
Date Mfgr Received | 2020-01-23 |
Date Added to Maude | 2020-02-06 |
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 | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
Manufacturer Street | 1852 10TH AVENUE |
Manufacturer City | COLUMBUS NE 68601 |
Manufacturer Country | US |
Manufacturer Postal Code | 68601 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BD NEEDLE 18X1-1/2 BLUNT FILL |
Generic Name | BLUNT FILL NEEDLE |
Product Code | GAA |
Date Received | 2020-02-06 |
Model Number | 305180 |
Catalog Number | 305180 |
Lot Number | 9226737 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
Manufacturer Address | 1852 10TH AVENUE COLUMBUS NE 68601 US 68601 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-06 |