MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2015-11-10 for URISYS 1100 03617556001 manufactured by Roche Diagnostics.
[30873375]
Patient Sequence No: 1, Text Type: N, H10
[30873376]
Reporter stated that the urisys 1100 reported negative results for leukocytes, while visual read of test strips showed values of 500 leukocytes/microliter. No adverse event was reported. The manufacturer requested the return of the suspect product for evaluation.
Patient Sequence No: 1, Text Type: D, B5
[35021643]
The customer did not return the urisys 1100 device so it could not be investigated. The urisys 1000 device was not returned.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1823260-2015-04500 |
MDR Report Key | 5213873 |
Report Source | COMPANY REPRESENTATIVE,OTHER |
Date Received | 2015-11-10 |
Date of Report | 2016-01-05 |
Date of Event | 2015-10-01 |
Date Mfgr Received | 2015-10-14 |
Date Added to Maude | 2015-11-10 |
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 | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
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 | URISYS 1100 |
Generic Name | AUTOMATED URINE ANALYZER |
Product Code | KHE |
Date Received | 2015-11-10 |
Model Number | NA |
Catalog Number | 03617556001 |
Lot Number | NA |
ID Number | NA |
Operator | NURSE |
Device Availability | N |
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 46250 US 46250 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-11-10 |