MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-17 for EFFLUENT BAG 107650 manufactured by Baxter Healthcare Corporation.
Report Number | 9610270-2020-00001 |
MDR Report Key | 9841695 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-17 |
Date of Report | 2020-03-17 |
Date of Event | 2020-02-04 |
Date Mfgr Received | 2020-02-20 |
Date Added to Maude | 2020-03-17 |
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 | PHARMACIST |
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 - MEDOLLA MODENA BLOOD |
Manufacturer Street | VIA MODENESE, 66 |
Manufacturer City | MEDOLLA MODENA 41036 |
Manufacturer Country | IT |
Manufacturer Postal Code | 41036 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EFFLUENT BAG |
Generic Name | SYSTEM, HEMODIALYSIS, REMOTE ACCESSORIES |
Product Code | MON |
Date Received | 2020-03-17 |
Model Number | NA |
Catalog Number | 107650 |
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 CORPORATION |
Manufacturer Address | DEERFIELD IL |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-17 |