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B. Braun Medical, Inc. recalls Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage: Th
Recalled May 5, 2021 · FDA recall Z-1509-2021 · B. Braun Medical
Hazard
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime. · FDA Class II
Units
1,900 units
Sold at
US Nationwide distribution in the states of NC, CA.
Description
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
Product
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.
Manufacturer(s)
B. Braun Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →