Baxter Healthcare Corp. Rt. Baxter Auto Syringe AS40 and AS40A Infusion Pump, product code 1M8565 (pumps with drug library option) and product codes 1M8560 and 1M8560R (pumps without drug library option); Baxter Healthcare Corporation, Medication Delivery Division, Deerfield, IL 60015 U.S.A. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Auto Syringe AS40 and AS40A Infusion Pump, product code 1M8565 (pumps with drug library option) and product codes 1M8560 and 1M8560R (pumps without drug library option); Baxter Healthcare Corporation, Medication Delivery Division, Deerfield, IL 60015 U.S.A.
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
all serial numbers
Products Sold
all serial numbers
Baxter Healthcare Corp. Rt. is recalling Baxter Auto Syringe AS40 and AS40A Infusion Pump, product code 1M8565 (pumps with drug library optio due to The occlusion detection and alarm may be delayed when the pumps are used with larger volume syringes at low flow rates.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The occlusion detection and alarm may be delayed when the pumps are used with larger volume syringes at low flow rates.
Recommended Action
Per FDA guidance
Important Product Information letters dated 2/8/06 were sent to the AS40 customers via first class mail to the attention of the Director of Nursing. The accounts were informed of the delay in the detection of a downstream occlusion when the AS40 pump is used with large volume syringes at low flow rates. To minimize the occlusion detection times at low flow rates, Baxter recommended that the customers take the following actions: * Use the smallest possible syringe size for the volume of fluid to be delivered; * Select the low occlusion pressure setting to minimize the detection time; * Utilize infusion sets with thick-walled, small bore tubing to minimize the detection time; and * Always verify that the clamping device or stopcock is open in the fluid path prior to starting an infusion.
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