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FDAMarch 15, 2021device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.

What to do

FDA enforcement status: Terminated

Brands named

b braun medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear