Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog Recalled by B. Braun Medical, Inc. Due to BBMI has identified through complaints the potential for...
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 B. Braun Medical, Inc. directly.
Affected Products
Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage: The extension set is a sterile, single-use intravascular direct injection, intermittent infusion, continuous infusion or aspiration of fluids and medications.
Quantity: 1,900 units
Why Was This Recalled?
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B. Braun Medical, Inc.
B. Braun Medical, Inc. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report