MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-10-24 for FISHER-SURE-VUE HCG-STAT SRM/URINE FHC-A202 23900530 manufactured by Alere San Diego.
| Report Number | 2027969-2019-00580 |
| MDR Report Key | 9234564 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2019-10-24 |
| Date of Report | 2019-11-22 |
| Date of Event | 2019-07-14 |
| Date Mfgr Received | 2019-11-13 |
| Date Added to Maude | 2019-10-24 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MONIKA BURRELL |
| Manufacturer Street | 9975 SUMMERS RIDGE ROAD |
| Manufacturer City | SAN DIEGO CA 92121 |
| Manufacturer Country | US |
| Manufacturer Postal | 92121 |
| Manufacturer Phone | 8588052084 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | FISHER-SURE-VUE HCG-STAT SRM/URINE |
| Generic Name | HCG PREGNANCY TEST |
| Product Code | JHI |
| Date Received | 2019-10-24 |
| Returned To Mfg | 2019-08-07 |
| Model Number | FHC-A202 |
| Catalog Number | 23900530 |
| Lot Number | HCG8120154 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ALERE SAN DIEGO |
| Manufacturer Address | 9995 SUMMERS RIDGE RD SAN DIEGO CA 92121 US 92121 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-10-24 |