CALCIUM
Report
- Report Number
- 1823260-2011-03907
- Event Type
- Malfunction
- Date Received
- July 23, 2011
- Date of Event
- June 30, 2011
- Report Date
- August 31, 2011
- Manufacturer
- ROCHE DIAGNOSTICS
- Product Code
- CIC
- PMA / PMN Number
- K061048
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
OTHER ASSAYS RELATED TO THIS EVENT ARE REPORTED IN MEDWATCH REPORTS WITH PATIENT IDENTIFIERS: (B)(6).
FURTHER INVESTIGATION COULD NOT BE PERFORMED AS ADDITIONAL INFORMATION WAS NOT PROVIDED. THE CUSTOMER CHANGED THE SAMPLE PROBE WHICH APPEARED TO RESOLVE THE ISSUE. THE ISSUE HAS NOT RECURRED. NO ADVERSE EVENTS WERE REPORTED.
THE USER RECEIVED QUESTIONABLE CALCIUM RESULTS FROM THE COBAS C501 SERIAL NUMBER (B)(4). OF THE DATA PROVIDED, THE RESULTS FOR ONE PATIENT SAMPLE WERE DISCREPANT. ALL RESULTS ARE IN MG/DL. THE INITIAL RESULT WAS 8.1 WITH A DATA FLAG. THE REPEAT RESULT ON ANOTHER COBAS C501 ANALYZER WAS 9.8. THE INITIAL RESULT WAS REPORTED OUTSIDE THE LABORATORY. THE USER REFUSED TO PROVIDE INFORMATION CONCERNING IF THE PATIENTS WERE ADVERSELY AFFECTED AS SHE STATED SHE HAD NO WAY TO DETERMINE THIS. NO CORRECTIVE REPORTS WERE GENERATED. UPON EVALUATION OF THE ANALYZER, THE FIELD SERVICE REPRESENTATIVE DETERMINED THERE WAS A FLUIDIC FAILURE OF THE SAMPLE PROBE. THE USER REPLACED THE SAMPLE PROBE. TO VERIFY THE ANALYZER OPERATION, THE FIELD SERVICE REPRESENTATIVE RAN CALIBRATION, QUALITY CONTROL AND PERFORMANCE TESTING WITH ALL RESULTS WITHIN SPECIFICATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CALCIUM | CRESOLPHTHALEIN COMPLEXONE, CALCIUM | CIC | ROCHE DIAGNOSTICS | NA | 64585701 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 088 YR |