Recall Z-0536-05 ยท GKZ Counter, Differential Cell
Beckman Coulter Inc
COULTER LH 750 Hematology Analyzer.
| Date | Feb 10, 2005 (initiated Dec 16, 2004) |
| Status | Terminated |
| Reason | A rare risk of sample misidentification exists with Coulter LH 750 Hematology Analyzers. The printout results from the instrument are affected; however, the results stored in the workstation's database are not affected. |
| Root cause | Other |
| Action | Letter 12/20/04 A rare risk of sample misidentification exists with Coulter LH 750 Hematology Analyzers. The printout results from the instrument are affected; however, the results stored in the workstation''s database are not affected. If the LH750 instrument displays a pop-up winder titled Database Error (XXXXXX) and text similar to (Microsoft) (ODBC SQL...) As soon as possible, call Beckman Coulter Customer Service, 800-526-7694) or contact your local rep, to schedule a service call. Do not acknowledge the error. Instead, restart the entire system by completely powering it OFF and then O |
| Quantity | 1,257 |
| Distribution | US and Canada |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.