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 2020-03-25 for FC 500 FLOW CYTOMETER FC500, RECOND TN, MCL UPS FLOW CYTOMETER 100-240V, A88262 manufactured by Beckman Coulter.
Report Number | 1061932-2020-00048 |
MDR Report Key | 9880464 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2020-03-25 |
Date of Report | 2020-03-25 |
Date of Event | 2020-03-13 |
Date Mfgr Received | 2020-03-13 |
Date Added to Maude | 2020-03-25 |
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. HARRY LONG |
Manufacturer Street | 1000 LAKE HAZELTINE DRIVE M/S R590C |
Manufacturer City | CHASKA MN 55318 |
Manufacturer Country | US |
Manufacturer Postal | 55318 |
Manufacturer Phone | 9523681224 |
Manufacturer G1 | BECKMAN COULTER |
Manufacturer Street | 11800 SW 147TH AVENUE |
Manufacturer City | MIAMI FL 331962031 |
Manufacturer Country | US |
Manufacturer Postal Code | 331962031 |
Single Use | 3 |
Remedial Action | RC |
Previous Use Code | 3 |
Removal Correction Number | 2050012-0108/2018-001C |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FC 500 FLOW CYTOMETER |
Generic Name | COUNTER, DIFFERENTIAL CELL |
Product Code | GKZ |
Date Received | 2020-03-25 |
Model Number | FC500, RECOND TN, MCL UPS FLOW CYTOMETER 100-240V, |
Catalog Number | A88262 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECKMAN COULTER |
Manufacturer Address | 250 S. KRAEMER BLVD. BREA CA 92821 US 92821 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-25 |