C.R. Bard, Inc. recalls Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S.

Recalled August 26, 2015 · FDA recall Z-2388-2015 · C.R. Bard

Hazard

Potential breach of the sterile barrier packaging. · FDA Class II

Units

534,972 each

Sold at

Nationwide Distribution-including AL, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI AND DC.

Description

Potential breach of the sterile barrier packaging.

Product

Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.

Manufacturer(s)

C.R. Bard, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →