I-Flow Corporation Easypump ST 100-1 infusion pump Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Easypump ST 100-1 infusion pump
Brand
I-Flow Corporation
Lot Codes / Batch Numbers
lot 562791
Products Sold
lot 562791
I-Flow Corporation is recalling Easypump ST 100-1 infusion pump due to The sterile pack may contain the wrong infusion pump inside.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The sterile pack may contain the wrong infusion pump inside.
Recommended Action
Per FDA guidance
The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.
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