MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-28 for UNSPECIFIED BD? SHARPS CONTAINER 305643 manufactured by Becton Dickinson Ind. Cirurgicas Ltda.
| Report Number | 3003916417-2019-00425 |
| MDR Report Key | 8941421 |
| Date Received | 2019-08-28 |
| Date of Report | 2019-09-19 |
| Date of Event | 2019-08-13 |
| Date Mfgr Received | 2019-08-13 |
| Device Manufacturer Date | 2018-05-17 |
| Date Added to Maude | 2019-08-28 |
| 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 | 0 |
| Brand Name | UNSPECIFIED BD? SHARPS CONTAINER |
| Generic Name | SHARPS CONTAINER |
| Product Code | MMK |
| Date Received | 2019-08-28 |
| Catalog Number | 305643 |
| Lot Number | 8137539 |
| Device Availability | N |
| Device Age | DA |
| 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 | 2019-08-28 |