MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-25 for MCKESSON CONSULT U120 URINE ANALYZER manufactured by Acon Laboratories, Inc..
| Report Number | 2531491-2020-00002 |
| MDR Report Key | 9752234 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2020-02-25 |
| Date of Report | 2020-01-28 |
| Date Mfgr Received | 2020-01-28 |
| Date Added to Maude | 2020-02-25 |
| 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. QIYI XIE |
| Manufacturer Street | 5850 OBERLIN DRIVE #340 |
| Manufacturer City | SAN DIEGO, CA |
| Manufacturer Country | US |
| Manufacturer Phone | 8758011 |
| Single Use | 3 |
| Remedial Action | RL |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MCKESSON CONSULT U120 URINE ANALYZER |
| Generic Name | URINE ANALYZER |
| Product Code | KQO |
| Date Received | 2020-02-25 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ACON LABORATORIES, INC. |
| Manufacturer Address | 5850 OBERLIN DRIVE #340 SAN DIEGO, CA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-25 |