Recall Z-2076-2025— C.R. Bard Inc

Name: FDA recall Z-2076-2025
Creator: U.S. Food and Drug Administration
Published: 2025-06-03

Class II · Ongoing

Class II FDA medical device recall by C.R. Bard Inc, initiated 2025-06-03. It names one FDA 510(k) clearance: K910846. Product: REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra. Reason: Cather packaging may contain the incorrect French size..

Recalling firm: C.R. Bard Inc
Classification: Class II
Status: Ongoing
Initiated: 2025-06-03
Firm location: Covington, GA, United States

510(k) clearances named in this recall

1 on FDA's record

K910846 — BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIFC.R. Bard, Inc.·cleared 1991-08-16

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra

Reason for recall

Cather packaging may contain the incorrect French size.

Data sourced from openFDA. This site is unofficial and independent of the FDA.