ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM
Report
- Report Number
- 2122870-2011-01002
- Event Type
- Injury
- Date Received
- April 15, 2011
- Date of Event
- March 17, 2011
- Report Date
- March 17, 2011
- Manufacturer
- BECKMAN COULTER, INC.
- Product Code
- MMI
- PMA / PMN Number
- K922823/A007
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
THE SAMPLE WAS COLLECTED IN A LITHIUM HEPARIN PLASMA TUBE WITH A GEL SEPARATOR. CENTRIFUGATION INFORMATION HAS NOT BEEN SUPPLIED TO DATE. QC IS PERFORMED ONCE EVERY 24 HOURS, AND WAS WITHIN THE ESTABLISHED RANGES PRIOR TO AND AFTER THE EVENT. A ROUTINE SYSTEM CHECK PERFORMED ON (B)(6) 2011 PASSED WITHIN INSTRUMENT SPECIFICATIONS. SERVICE WAS NOT DISPATCHED FOR THIS EVENT AS THE CUSTOMER HAS THEIR OWN BIO-MEDICAL ENGINEER (BME). BCI HAS MADE SEVERAL UNSUCCESSFUL ATTEMPTS TO CONTACT THE CUSTOMER FOR ADDITIONAL INFORMATION. HARDWARE VERIFICATION INFORMATION HAS NOT BEEN SUPPLIED TO DATE. A DEFINITIVE ROOT CAUSE HAS NOT BEEN DETERMINED TO DATE FOR THIS EVENT WITH THE DATA PROVIDED.
A CUSTOMER CONTACTED BECKMAN COULTER, INC. (BCI) IN REGARDS TO AN ERRONEOUSLY ELEVATED TROPONIN (ACCUTNI) RESULT, ABOVE THE AMI CUTOFF, GENERATED BY ACCESS 2 IMMUNOASSAY SYSTEM FOR ONE PATIENT. THE RESULT WAS REPORTED OUT OF THE LABORATORY. SUBSEQUENT TESTING ON AN ALTERNATE INSTRUMENT PRODUCED A LOWER RESULT WITHIN THE NORMAL REFERENCE RANGE. THE PATIENT WAS TREATED WITH MEDICATION BUT THE SPECIFIC MEDICATION AND DOSAGE HAS NOT BEEN SUPPLIED TO DATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM | DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER | MMI | BECKMAN COULTER, INC. | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |