Baxter Healthcare Corporation EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar.
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
Product Code: ADS201897. Lot Numbers: 0000266641, 0000325839, 0000362640, 0000380266.
Products Sold
Product Code: ADS201897. Lot Numbers: 0000266641, 0000325839, 0000362640, 0000380266.
Baxter Healthcare Corporation is recalling EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar. due to There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date
Recommended Action
Per FDA guidance
On June 15th 2021, the firm sent a letter to its customers with the following instructions: 1. Healthcare providers may continue to safely use the EASYGRIP FLO-41 delivery system while following the human readable expiry date printed on the primary and secondary package labeling, which are also listed in the table above. 2. If you received this communication directly from Baxter, complete the enclosed Baxter customer reply form and return it to Baxter by e-mailing it to fca@baxter.com, even if you do not have any inventory. Returning the customer reply form promptly will confirm your receipt of this notification and prevent you from receiving repeat notices. If you do not return the customer reply form, you will receive a phone call from OnProcess Technology on behalf of Baxter to confirm your receipt of this notification. 3. If you distribute this product to other facilities or departments within your institution, please forward a copy of this communication to them.
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