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 2020-01-27 for BD DISPOSABLE CORNWALL SYRINGE SYSTEM 305224 manufactured by Bd Infusion Therapy Systems Inc. S.a. De C.v..
Report Number | 9610847-2020-00018 |
MDR Report Key | 9632592 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
Date Received | 2020-01-27 |
Date of Report | 2020-01-21 |
Date of Event | 2020-01-02 |
Date Mfgr Received | 2020-01-02 |
Device Manufacturer Date | 2018-02-06 |
Date Added to Maude | 2020-01-27 |
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 |
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 INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Street | PERIFERICO LUIS DONALDO COLOSIO NO. 579 |
Manufacturer City | NOGALES |
Manufacturer Country | MX |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BD DISPOSABLE CORNWALL SYRINGE SYSTEM |
Generic Name | SYRINGE SYSTEM |
Product Code | KYX |
Date Received | 2020-01-27 |
Catalog Number | 305224 |
Lot Number | 8019542 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Address | PERIFERICO LUIS DONALDO COLOSIO NO. 579 NOGALES MX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-01-27 |