Z-2076-2025 Class II Ongoing
FDA device recall Z-2076-2025 was initiated by C.R. Bard Inc on June 3, 2025 and is designated Class II. Reason for recall: Cather packaging may contain the incorrect French size. The recall status is ongoing. Affected quantity: 63 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 9, 2025
- Initiation Date
- June 3, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 63 units
Product Description
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Reason for Recall
Cather packaging may contain the incorrect French size.
Distribution Pattern
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.
Code Information
Lot # NGJX2513/UDI: 00801741000294