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 2018-12-19 for ELECSYS AMH SYSTEM 06331076190 manufactured by Roche Diagnostics.
[131178394]
This event occurred in (b)(6).
Patient Sequence No: 1, Text Type: N, H10
[131178395]
The customer complained of a questionable elecsys amh result for 1 patient sample tested on a cobas e 411 immunoassay analyzer serial number (b)(4). The initial amh result on the e 411 was 2. 74 pmol/l. On (b)(6) 2018 the sample was repeated in a different laboratory and the amh result 30. 3 pmol/l. The specific analyzer was asked for but not provided. The customer did not believe that the result on the e 411 was correct. There was no allegation of an adverse event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1823260-2018-05009 |
MDR Report Key | 8179633 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2018-12-19 |
Date of Report | 2019-01-14 |
Date of Event | 2018-09-14 |
Date Mfgr Received | 2018-12-07 |
Date Added to Maude | 2018-12-19 |
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 | 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 AMH SYSTEM |
Generic Name | ANTI-M?LLERIAN HORMONE TEST SYSTEM |
Product Code | PQO |
Date Received | 2018-12-19 |
Model Number | NA |
Catalog Number | 06331076190 |
Lot Number | 238131 |
Device Expiration Date | 2018-04-30 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
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 | 2018-12-19 |