FDA Medical devices recall ·
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra recall
- Recall number
- Z-2076-2025
- Date
- (initiated June 3, 2025)
- Company / brand
- C.R. Bard Inc
8195 Industrial Blvd Ne, Covington, GA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 63 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Why was it recalled?
Cather packaging may contain the incorrect French size.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot # NGJX2513/UDI: 00801741000294
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: Alabama Arkansas Arizona California Colorado Florida Georgia Illinois Indiana Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Vermont Wisconsin West Virginia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2076-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.