C.R. Bard, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2386-2015)

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 Catheters (6"), 14 Fr, (30/box), Product Code 51614. Intermittent catheter.

Product Classification:

Class II

Date Initiated: July 7, 2015

Date Posted: August 26, 2015

Recall Number: Z-2386-2015

Event ID: 71722

Reason for Recall:

Potential breach of the sterile barrier packaging.

Status: Terminated

Product Quantity: 37,686 each

Code Information:

Lot Number 73600003, 73600006, 7360007, 73600011, 73600012, 73600013, 73600016, 73600017, 73600020, 73600021, 73600024, 73600080, 73600081, 73600082, 73600095, 73600096, 73600097, 73600123, 73600124, 73600125, 73600126, 73600144, 73600145, 73600163, 73600164, 73600167, 73600181, 73600196, 73600217, 73600218

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