Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female Recalled by C.R. Bard, Inc. Due to Specific lots labeled as an Antibacterial Hydrophilic Intermittent...
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 C.R. Bard, Inc. directly.
Affected Products
Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.
Quantity: 45,270 units
Why Was This Recalled?
Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating.
Where Was This Sold?
This product was distributed to 23 states: AL, AZ, CA, FL, GA, IL, IN, KS, KY, MA, MO, NJ, NY, NC, OH, OK, OR, PA, TN, TX, UT, VA, WA
About C.R. Bard, Inc.
C.R. Bard, Inc. has 51 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report