Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
WHIN Infusion Set - 90 Huber Needle and Wing (22 Recalled by B. Braun Medical, Inc. Due to Potential for the tip of the Huber needle...
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
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units per case, Catalog Number 471734. Usage: Infusion of solution/medication into implanted intravascular ports.
Quantity: 5,980 units [Lot # 0061482060 (3,340 units); Lot # 0061486821 (2,640 units)]
Why Was This Recalled?
Potential for the tip of the Huber needle on the WHIN Infusion Set to protrude from the needle guard.
Where Was This Sold?
This product was distributed to 18 states: AL, AR, CA, FL, GA, IL, IN, KY, MA, MS, NV, NJ, OH, PA, SC, TN, TX, VA
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