Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude 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 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter
Quantity: 8,970 each
Why Was This Recalled?
Potential breach of the sterile barrier packaging.
Where Was This Sold?
This product was distributed to 14 states: CA, FL, IL, MA, MN, NH, NJ, NY, NC, OH, OK, PA, TX, 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