C.R. Bard, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2732-2015)

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 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter

Product Classification:

Class II

Date Initiated: August 24, 2015

Date Posted: September 9, 2015

Recall Number: Z-2732-2015

Event ID: 72024

Reason for Recall:

Potential breach of the sterile barrier packaging.

Status: Terminated

Product Quantity: 8,970 each

Code Information:

Lot Number 53621456

Distribution Pattern:

US Distribution to states of:CA, FL, IL, MA, MN, NH, NJ, NY, NC, OH, OK, PA, TX, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated