Baxter Healthcare Corp. Rt. Clinician Workstation Software, product code 2M5042 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Clinician Workstation Software, product code 2M5042
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
Product code 2M5042, software versions 3.4, 4.0 and 4.1
Products Sold
Product code 2M5042, software versions 3.4, 4.0 and 4.1
Baxter Healthcare Corp. Rt. is recalling Clinician Workstation Software, product code 2M5042 due to The medication administration results displayed in the 'View Results' link may be inaccurate.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The medication administration results displayed in the 'View Results' link may be inaccurate.
Recommended Action
Per FDA guidance
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 to be used as the primary source of information for reviewing medication adminstration results. The accounts were instructed to contact their account executive and/or the Client Support Services at 1-877-835-2727 for instructions on how to disable the 'View Results' feature.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, MA, MO, VT
Page updated: Jan 10, 2026