Class II

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

C.R. Bard Inc · June 3, 2025

Reason for Recall

Cather packaging may contain the incorrect French size.

Distribution

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, FL, GA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WI, WV and the country of Canada.

States Affected

NATIONWIDE

Quantity Affected

63 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2076-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.