Recall Z-0981-05 ยท LNX
Baxter Healthcare Corp.
Clinician Workstation Software, product code 2M5042
| Date | Jul 13, 2005 (initiated Mar 10, 2005) |
| Status | Terminated |
| Reason | The medication administration results displayed in the 'View Results' link may be inaccurate. |
| Root cause | Other |
| Action | Urgent Device Correction recall letters dated 3/10/05 were sent to the direct accounts on the same date via first class mail. The letter describes the inaccuracies in the 'View Results' program, and informed the accounts that inaccurate information could lead to incorrect clinical decision-making, which could impact a patient''s medication treatment protocol. The accounts were requested to disable the 'View Results' link until a software upgrade is available, and to inform all clinical point of care users that the 'View Results' has been disabled and that the Manual Adminstration Record is t |
| Quantity | 5 units |
| Distribution | Missouri, Massachusetts, Vermont, California and Canada. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.