C.R. Bard, Inc. recalls Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermitte

Recalled August 26, 2015 · FDA recall Z-2384-2015 · C.R. Bard

Hazard

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

Units

14,310 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 Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent catheter.

Manufacturer(s)

C.R. Bard, Inc.

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