Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Recalled by C.R. Bard, Inc. Due to Potential breach of the sterile barrier packaging.
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
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.
Quantity: 534,972 each
Why Was This Recalled?
Potential breach of the sterile barrier packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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