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 2020-03-23 for COULTER LH 750 HEMATOLOGY ANALYZER 6605632 manufactured by Beckman Coulter.
| Report Number | 1061932-2020-01933 |
| MDR Report Key | 9866519 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
| Date Received | 2020-03-23 |
| Date of Report | 2020-03-23 |
| Date of Event | 2018-04-17 |
| Date Mfgr Received | 2018-04-17 |
| Device Manufacturer Date | 2004-02-01 |
| Date Added to Maude | 2020-03-23 |
| 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 |
| Manufacturer Country | US |
| Manufacturer Phone | 3681224 |
| Manufacturer G1 | BECKMAN COULTER |
| Manufacturer Street | 11800 SW 147TH AVENUE |
| Manufacturer City | MIAMI, FL |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COULTER LH 750 HEMATOLOGY ANALYZER |
| Generic Name | COUNTER, DIFFERENTIAL CELL |
| Product Code | GKZ |
| Date Received | 2020-03-23 |
| Model Number | 750 |
| Catalog Number | 6605632 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECKMAN COULTER |
| Manufacturer Address | 250 S. KRAEMER BLVD. BREA, FL US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-23 |