Baxa Corporation Pharmacy compounding system . It is a twenty-four source compounder for multi-source fluid mixing of both macro and micro ingredient down to 0.2 ml quantities. Product Usage: Pharmacy compounding System for parenteral macro and micro ingredients Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pharmacy compounding system . It is a twenty-four source compounder for multi-source fluid mixing of both macro and micro ingredient down to 0.2 ml quantities. Product Usage: Pharmacy compounding System for parenteral macro and micro ingredients
Brand
Baxa Corporation
Lot Codes / Batch Numbers
2 model numbers 2400 D and 2400 M.
Products Sold
2 model numbers 2400 D and 2400 M.
Baxa Corporation is recalling Pharmacy compounding system . It is a twenty-four source compounder for multi-source fluid mixing of due to Software issue with compounding pump resulting in over delivery of component ingredients during routine operations.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software issue with compounding pump resulting in over delivery of component ingredients during routine operations.
Recommended Action
Per FDA guidance
Baxa sent a Safety Alert letter dated March 23, 2009 to all affected consignees. The letter identified the affected product, problem and recommended actions with specific instructions related to the issue. Additionally, the firm will be providing a warning label for the affected product as soon as possible and is currently working on a product upgrade to correct the issue. For assistance contact Baxa Technical Support at 800-678-2292. The firm is also providing a 24 hour a day, 7 days a week Technical Support for the affected product.
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 noticePage updated: Jan 10, 2026