MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-11-15 for ACCESS VITAMIN B12 REAGENT 33000 manufactured by Beckman Coulter.
Report Number | 2122870-2019-01140 |
MDR Report Key | 9329281 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2019-11-15 |
Date of Report | 2019-11-15 |
Date of Event | 2019-10-30 |
Date Facility Aware | 2019-11-01 |
Date Mfgr Received | 2019-11-01 |
Device Manufacturer Date | 2019-06-01 |
Date Added to Maude | 2019-11-15 |
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 | MR. DAVID DAVIS |
Manufacturer Street | 250 S. KRAEMAR BLVD. |
Manufacturer City | BREA CA 928218000 |
Manufacturer Country | US |
Manufacturer Postal | 928218000 |
Manufacturer Phone | 7149613796 |
Manufacturer G1 | BECKMAN COULTER |
Manufacturer Street | 1000 LAKE HAZELTINE DRIVE |
Manufacturer City | CHASKA MN 55318 |
Manufacturer Country | US |
Manufacturer Postal Code | 55318 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ACCESS VITAMIN B12 REAGENT |
Generic Name | RADIOASSAY, VITAMIN B12 |
Product Code | CDD |
Date Received | 2019-11-15 |
Model Number | 33000 |
Catalog Number | 33000 |
Lot Number | 921022 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECKMAN COULTER |
Manufacturer Address | 1000 LAKE HAZELTINE DRIVE CHASKA MN 55318 US 55318 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-15 |