BECKMAN COULTER LAB AUTOMATION SYSTEM
Report
- Report Number
- 2050012-2011-06057
- Event Type
- Malfunction
- Date Received
- October 14, 2011
- Date of Event
- September 16, 2011
- Report Date
- September 16, 2011
- Manufacturer
- BECKMAN COULTER BIOMEDICAL GMBH
- Product Code
- JQP
- PMA / PMN Number
- EXEMPT
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
Narratives
A FIELD SERVICE ENGINEER (FSE) WENT ON-SITE AND IMPLEMENTED BEC APPROVED LABELS. FSE CHECKED THE CUSTOMER'S STOCK AND INSTRUCTED CUSTOMER TO REMOVE ALL STOCK OF NON-APPROVED LABEL ROLLS (ABOUT 100 LABEL ROLLS). A SERVICE VISIT WAS SCHEDULED TO INSTALL A SECOND BARCODE READER. (B)(4).
A CUSTOMER CONTACTED BECKMAN COULTER INC. (BEC) REGARDING AN EVENT THAT OCCURRED AS A RESULT OF PRINTING ERRORS CAUSED BY OPERATING THE AUTOMATE 2500 SYSTEM WITH NON BEC APPROVED LABELS. TWO DIFFERENT BARCODE LABELS WERE FOUND ATTACHED TO ONE SECONDARY TUBE. THE SECOND LABEL WAS DIRECTLY ATTACHED OVER THE FIRST LABEL. THE BARCODE LABELS WERE NOT FROM BEC. THE ERROR MESSAGE THAT WAS DISPLAYED BY THE SYSTEM AFTER THE UNSUCCESSFUL ATTEMPT TO APPLY A LABEL TO THE SECONDARY TUBE WAS NOT CORRECTLY FOLLOWED AND THE PRINTER WAS NOT ADEQUATELY INSPECTED. NO INCORRECT RESULTS WERE REPORTED OUTSIDE OF THE LABORATORY SINCE THE LABORATORY STAFF NOTICED THE DOUBLE LABELED TUBE AND PREVENTED IT FROM FURTHER PROCESSING AND CONDUCTED TESTING WITH THE ORIGINAL TUBE (PRIMARY TUBE). THERE WAS NO AFFECT TO PATIENTS WITH REGARD TO THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BECKMAN COULTER LAB AUTOMATION SYSTEM | CALCULATOR/DATA PROCESSING MODULE FOR CLINICAL USE | JQP | BECKMAN COULTER BIOMEDICAL GMBH | AUTOMATE 2500 S3I | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |