B. Braun Medical, Inc. 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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
B. Braun Medical, Inc.
Lot Codes / Batch Numbers
Lot #: 00SL713784, 0061741483, 0061755034, 0061755296
Products Sold
Lot #: 00SL713784, 0061741483, 0061755034, 0061755296
B. Braun Medical, Inc. is recalling Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 due to BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
Recommended Action
Per FDA guidance
On 03/12/2021, B. Braun issued an Urgent Medical Device Recall notice via letter notifying customers of the potential for the extension set to become occluded or unable to prime.
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