Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Drainer(R) Centesis Catheters: (a) REF 8810 Recalled by Vascular Solutions, Inc. Due to The supplier of Drainer(R) centesis catheters notified Vascular...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Vascular Solutions, Inc. directly.
Affected Products
Drainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8812, 5F x 15cm Product The Drainer centesis catheter is intended for use in percutaneous fluid aspirations and small volume drainage procedures.
Quantity: 276 units
Why Was This Recalled?
The supplier of Drainer(R) centesis catheters notified Vascular Solutions, Inc. that there is a potential for certain production lots to contain unsafe levels of bacterial endotoxins.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Vascular Solutions, Inc.
Vascular Solutions, Inc. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report