MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2020-02-03 for ORALPAK 3ML BLUE HOSPITAL 990091 manufactured by Becton Dickinson Ind. Cirurgicas Ltda.
Report Number | 3003916417-2020-00019 |
MDR Report Key | 9660489 |
Report Source | FOREIGN,OTHER |
Date Received | 2020-02-03 |
Date of Report | 2020-01-15 |
Date of Event | 2020-01-09 |
Date Mfgr Received | 2020-01-13 |
Device Manufacturer Date | 2019-01-24 |
Date Added to Maude | 2020-02-03 |
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 IND. CIRURGICAS LTDA |
Manufacturer Street | 550 RUA CYRO CORREIA PEREIRA |
Manufacturer City | CURITIBA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ORALPAK 3ML BLUE HOSPITAL |
Generic Name | ORALPAK |
Product Code | KYX |
Date Received | 2020-02-03 |
Catalog Number | 990091 |
Lot Number | 9024719 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON DICKINSON IND. CIRURGICAS LTDA |
Manufacturer Address | 550 RUA CYRO CORREIA PEREIRA CURITIBA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-03 |