Recall Z-0613-2024 ยท JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
Abbott Laboratories
Alinity ci-series System Control Module, REF: 03R70-01
| Date | Dec 22, 2023 (initiated May 30, 2023) |
| Status | Open, Classified |
| Reason | There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error during daily maintenance; 2) Sample Laboratory Report error; 3) Customer requests mechanism to prevent user error when creating new lots of value assigned Calibrators; 4) Error in processing tests after CCCintController encountered an error with the assay information downloaded from SCC; 5) The assay editor does not correctly check sample dilution total volume limits; 6) User-Applied Labels not adhering to Reagent Bottles; 7) ICT Module did not ex |
| Root cause | Software design |
| Action | On 5/30/23, correction notices were mailed to customers: -If code 5819 occurs, remove cartridges and onboard vial rack. Discard all cartridges and all samples in the onboard vial racks impacted by this issue. If a cartridge or onboard vial rack has fallen over inside the reagent carousel, contact Customer Service to clean any potential spill. -Avoid printing the Sample Laboratory report from the Sample Status Screen. If the Sample Laboratory report is printed verify the correct SID is printed on all pages. -When the barcode on the calibrator carton is scanned, only the master lot number and |
| Quantity | 8,424 |
| Distribution | US: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV OUS: ALBANIA, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHAMAS, BAHRAIN, BANGLADESH, BELARUS, BELGIUM, BERMUDA, |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.