MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-03-01 for RF-II RHEUMATOID FACTORS II 05480167190 manufactured by Roche Diagnostics.
[101596470]
(b)(4). (b)(6).
Patient Sequence No: 1, Text Type: N, H10
[101596531]
The customer received questionable rf-ii rheumatoid factors ii results for one patient sample. The result from cobas 8000 c 702 module serial number (b)(4) was 39. 8 iu/ml. The result from a au580 analyzer 1152 iu/ml. The results from a immage 800 analyzer was 750. 0 iu/ml. The customer diluted the sample 1:5 and the result was 11. 3 (56. 5) iu/ml. No erroneous result was reported outside of the laboratory. There was no allegation of an adverse event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1823260-2018-00620 |
| MDR Report Key | 7306819 |
| Date Received | 2018-03-01 |
| Date of Report | 2018-05-14 |
| Date of Event | 2018-02-09 |
| Date Mfgr Received | 2018-02-10 |
| Date Added to Maude | 2018-03-01 |
| 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 | 0 |
| Brand Name | RF-II RHEUMATOID FACTORS II |
| Generic Name | SYSTEM, TEST, RHEUMATOID FACTOR |
| Product Code | DHR |
| Date Received | 2018-03-01 |
| Model Number | NA |
| Catalog Number | 05480167190 |
| Lot Number | 27266201 |
| ID Number | NA |
| Device Expiration Date | 2019-08-31 |
| 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 | 2018-03-01 |