MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-26 for CARTRIDGE manufactured by Baxter Healthcare - Tijuana Baja.
Report Number | 8030638-2019-00018 |
MDR Report Key | 9375784 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-11-26 |
Date of Report | 2019-11-26 |
Date Facility Aware | 2019-11-03 |
Report Date | 2019-11-25 |
Date Reported to FDA | 2019-11-25 |
Date Reported to Mfgr | 2019-11-25 |
Date Mfgr Received | 2019-11-03 |
Date Added to Maude | 2019-11-26 |
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 Street | 25212 W. ILLINOIS ROUTE 120 |
Manufacturer City | ROUND LAKE IL 60073 |
Manufacturer Country | US |
Manufacturer Postal | 60073 |
Manufacturer Phone | 2242702068 |
Manufacturer G1 | BAXTER HEALTHCARE - TIJUANA BAJA |
Manufacturer Street | BLVD PACIFICO 10014 PARQUE INDUSTRIAL PACIFICO |
Manufacturer City | TIJUANA BAJA CALIFORNIA CP 22643 |
Manufacturer Country | MX |
Manufacturer Postal Code | CP 22643 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CARTRIDGE |
Generic Name | SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE |
Product Code | FJK |
Date Received | 2019-11-26 |
Model Number | NA |
Catalog Number | ASKU |
Lot Number | ASKU |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAXTER HEALTHCARE - TIJUANA BAJA |
Manufacturer Address | DEERFIELD IL |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-26 |