C.R. Bard, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2388-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 7, 2015

Date Posted: August 26, 2015

Recall Number: Z-2388-2015

Event ID: 71722

Reason for Recall:

Potential breach of the sterile barrier packaging.

Status: Terminated

Product Quantity: 534,972 each

Code Information:

Lot Number 53620387, 53621274, 53621279

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated