Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to Incorrect unit labeling. The case label and shelf...

Date: October 2, 2015
Company: C.R. Bard, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact C.R. Bard, Inc. directly.

Affected Products

Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units

Quantity: 4,170 each

Why Was This Recalled?

Incorrect unit labeling. The case label and shelf box are correct, Product Code 63512 and Catheter Size 12 French. The unit label (catheter package) may state Product Code 63516 and Catheter Size 16 French.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About C.R. Bard, Inc.

C.R. Bard, Inc. has 51 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report