MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other,user facility report with the FDA on 2020-02-17 for PHASEAL PROTECTOR P53 515107 manufactured by Becton Dickinson, S.a..
Report Number | 3003152976-2020-00062 |
MDR Report Key | 9718045 |
Report Source | FOREIGN,OTHER,USER FACILITY |
Date Received | 2020-02-17 |
Date of Report | 2020-01-30 |
Date of Event | 2020-01-15 |
Date Mfgr Received | 2020-01-28 |
Device Manufacturer Date | 2017-06-26 |
Date Added to Maude | 2020-02-17 |
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, S.A. |
Manufacturer Street | CAMINO DE VALDEOLIVIA S/N |
Manufacturer City | SAN AGUSTIN DE GUADALIX |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PHASEAL PROTECTOR P53 |
Generic Name | INTRAVASCULAR ADMINISTRATION SET |
Product Code | ONB |
Date Received | 2020-02-17 |
Model Number | 515107 |
Catalog Number | 515107 |
Lot Number | 1704010 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON DICKINSON, S.A. |
Manufacturer Address | CAMINO DE VALDEOLIVIA S/N SAN AGUSTIN DE GUADALIX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-17 |