MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-25 for LI LITHIUM manufactured by Roche Diagnostics.
[134750791]
The investigation found that the calibration results were inconspicuous and the qc results were acceptable, a general reagent or instrument issue can be excluded. The sample was submitted for investigation and the customer's results could be confirmed. The follow up/corrective actions were not provided. No devices were returned. This device is not labeled for single use and is not reprocessed or reused.
Patient Sequence No: 1, Text Type: N, H10
[134750792]
This report summarizes 1 malfunction events. Erroneous low results were generated by the cobas 6000 c (501) module. The event involved 1 patient with erroneous results for li lithium that did not correlate with the patient's treatment. The patient's age was (b)(6). The patient's gender was male. The patient's race was requested but was not provided. The patient's ethnicity was requested but was not provided.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1823260-2019-90020 |
| MDR Report Key | 8278635 |
| Date Received | 2019-01-25 |
| Date Added to Maude | 2019-01-25 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | 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 | SANDHOFFERSTRASSE 116 NA |
| Manufacturer City | MANNHEIM (BADEN-WURTTEMBERG), NA 68305 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 68305 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | LI LITHIUM |
| Generic Name | LITHIUM TEST SYSTEM |
| Product Code | NDW |
| Date Received | 2019-01-25 |
| Model Number | LITHIUM |
| Lot Number | 29913401 |
| Device Availability | * |
| Device Age | DA |
| Device Eval'ed by Mfgr | * |
| 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 | 2019-01-25 |