C.R. Bard, Inc.: Medical Device Recall in 2017 - (Recall #: Z-3226-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.

Product Classification:

Class II

Date Initiated: July 28, 2017

Date Posted: October 4, 2017

Recall Number: Z-3226-2017

Event ID: 78031

Reason for Recall:

Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating.

Status: Terminated

Product Quantity: 45,270 units

Code Information:

Catalog No. 51514; Lot No. 53623024, 53623054, 53623047, 53623122; Exp Date 01/31/2020

Distribution Pattern:

Distribution to AL, AZ, CA, FL, GA, IL, IN, KS, KY, MA, MO, NC, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA.

Voluntary or Mandated:

Voluntary: Firm initiated