Baxter Healthcare Corp. Rt. Logix-CM Compounder Software, catalog 2M8400; Baxter Healthcare Corporation, Medication Delivery System, Round Lake, IL 60073 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Logix-CM Compounder Software, catalog 2M8400; Baxter Healthcare Corporation, Medication Delivery System, Round Lake, IL 60073
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
Software version 3.0.4
Products Sold
Software version 3.0.4
Baxter Healthcare Corp. Rt. is recalling Logix-CM Compounder Software, catalog 2M8400; Baxter Healthcare Corporation, Medication Delivery Sys due to Logix-CM software version 3.0.4 has not completed its official release process.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Logix-CM software version 3.0.4 has not completed its official release process.
Recommended Action
Per FDA guidance
Urgent Product Recall letters dated 12/20/04 were sent to the end users via overnight mail. The accounts were informed that software version 3.0.4 has not been officially released and must be removed from their compounders. They were requested to complete and fax the customer reply form to Baxter at 847-270-5457, indicating if they are currently using Logix-CM software. Upon receipt of the reply form, Baxter will schedule a visit to the facility to remove Logix-CM software version 3.0.4 from their compounder and revert the software back to the configuration prior to Logix-CM 3.0.4 placement. Any questions were directed to Baxter Clintec Nutrition, option 1, at 1-800-422-2751.
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
AZ, CA, NC, UT, WI
Page updated: Jan 10, 2026