Baxter Healthcare Corp. Rt. Logix TPN Software Solution, catalog 2M8410, consists of the Logix Order Entry (OE) Installation CD, version 1.0.28 and Logix Compounder Manager (CM) Installation CD, version 3.1.8. The software is included in a number of Baxter's pharmacy compounders. The software assists the pharmacist in management of compounding, creating and authorizing nutritional solutions intended for IV administration. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Logix TPN Software Solution, catalog 2M8410, consists of the Logix Order Entry (OE) Installation CD, version 1.0.28 and Logix Compounder Manager (CM) Installation CD, version 3.1.8. The software is included in a number of Baxter's pharmacy compounders. The software assists the pharmacist in management of compounding, creating and authorizing nutritional solutions intended for IV administration.
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
Software version 1.0.2 (comprised of Logix OE version 1.0.28 and Logix CM version 3.1.8)
Products Sold
Software version 1.0.2 (comprised of Logix OE version 1.0.28 and Logix CM version 3.1.8)
Baxter Healthcare Corp. Rt. is recalling Logix TPN Software Solution, catalog 2M8410, consists of the Logix Order Entry (OE) Installation CD, due to Software anomaly results in inaccurate information being printed out on the Delivery Report, even though the compounder performed the compounding corr. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software anomaly results in inaccurate information being printed out on the Delivery Report, even though the compounder performed the compounding correctly.
Recommended Action
Per FDA guidance
Baxter sent the 3/28/08 Urgent Device Correction letter to affected customers, to the attention of the Director of Pharmacy, via first class mail to advise them of the potential inaccuracy of the Delivery Report due to a software anomaly. The accounts were instructed to review each delivery report for accuracy. If the report contains zero actual volumes the user must manually reprint the report. The letter outlined the process for reprinting the Delivery Report. Any questions were directed to the Baxter Nutritional Professional Services at 1-800-422-2751. The accounts were requested complete the enclosed reply form acknowledging receipt and understanding of the letter and dissemination of the information to their staff. A software upgrade will be provided. If you have questions about this letter or you did not receive this letter contact Baxter Nutrition Professional Services 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, MN, WI, PR
Page updated: Jan 10, 2026