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C.R. Bard, Inc. recalls Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are
Recalled September 9, 2015 · FDA recall Z-2732-2015 · C.R. Bard
Hazard
Potential breach of the sterile barrier packaging. · FDA Class II
Units
8,970 each
Sold at
US Distribution to states of:CA, FL, IL, MA, MN, NH, NJ, NY, NC, OH, OK, PA, TX, and WA.
Description
Potential breach of the sterile barrier packaging.
Product
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
Manufacturer(s)
C.R. Bard, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →