Vascular Solutions, Inc. The Pronto Extraction Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The Pronto Extraction Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system.
Brand
Vascular Solutions, Inc.
Lot Codes / Batch Numbers
lot numbers S000121, S000122, 300748, 300783, 300784, 300792, and 300822.
Products Sold
lot numbers S000121, S000122, 300748, 300783, 300784, 300792, and 300822.
Vascular Solutions, Inc. is recalling The Pronto Extraction Catheter is indicated for the removal of fresh, soft emboli and thrombi from v due to The marker band in guidewire lumen could move from the manufactured location during clinical use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The marker band in guidewire lumen could move from the manufactured location during clinical use.
Recommended Action
Per FDA guidance
letter 5/21/2004, representative visit to foreign accounts.
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