C.R. Bard, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2830-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Option-vf Urinary Catheter. Female use only. Latex Free. Sterile, Rx only.

Product Classification:

Class II

Date Initiated: July 11, 2016

Date Posted: September 21, 2016

Recall Number: Z-2830-2016

Event ID: 74712

Reason for Recall:

During an FDA inspection it was found out that the Practical Foley Catheters to be potentially nonsterile.

Status: Terminated

Product Quantity: 274 units

Code Information:

Device Listing No.: D022512. CatalogNo.: FV14218. Lot No.: P1007637, P1007638, P1007461. Exp Date: 08/01/2016.

Distribution Pattern:

US Distribution to the states of : AL, CA, CO, FL, IL, IN, MA, MD, NJ, NY, OR, PA, TN, WA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated