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 2016-11-09 for ELECSYS AFP ASSAY 04491742190 manufactured by Roche Diagnostics.
[59459903]
(b)(4). (b)(6).
Patient Sequence No: 1, Text Type: N, H10
[59459904]
The customer received a questionable high elecsys afp assay result for one patient sample from cobas 8000 (e602) serial number (b)(4). The initial result with a dilution was 1,603,000 ng/ml. The result from a centaur analyzer was 800 ng/ml. The sample was submitted for investigation as the customer suspected a nonspecific reaction. With an unknown roche analyzer, the high result was reproduced at 991,700 ng/ml with a 1:1000 dilution. The results with lumipulse and fuji-rebio methods were >50,000 ng/ml. Information concerning if any erroneous result was reported outside the laboratory was requested but it was unknown. The patient was not adversely affected.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1823260-2016-01750 |
| MDR Report Key | 6088832 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
| Date Received | 2016-11-09 |
| Date of Report | 2016-11-09 |
| Date of Event | 2016-10-16 |
| Date Mfgr Received | 2016-10-27 |
| Date Added to Maude | 2016-11-09 |
| 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 | NA MICHAEL LESLIE |
| Manufacturer Street | 9115 HAGUE ROAD NA |
| Manufacturer City | INDIANAPOLIS IN 46250 |
| Manufacturer Country | US |
| Manufacturer Postal | 46250 |
| Manufacturer Phone | 3175214343 |
| Manufacturer G1 | ROCHE DIAGNOSTICS GMBH |
| Manufacturer Street | SANDHOFERSTRASSE 116 NA |
| Manufacturer City | MANNHEIM (BADEN-WURTTEMBERG) 68305 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 68305 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ELECSYS AFP ASSAY |
| Generic Name | KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER |
| Product Code | LOJ |
| Date Received | 2016-11-09 |
| Model Number | NA |
| Catalog Number | 04491742190 |
| Lot Number | 120174 |
| ID Number | NA |
| Device Expiration Date | 2017-06-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ROCHE DIAGNOSTICS |
| Manufacturer Address | 9115 HAGUE ROAD NA INDIANAPOLIS IN 462500457 US 462500457 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-11-09 |