C.R. Bard Urologist's Tray Recall: Incorrect French Size Packaging
C.R. Bard recalls urologist's trays with incorrect French size packaging. This may lead to improper use during procedures. Affected units include specific lot numbers.
Lower-risk recall
Cather packaging may contain the incorrect French size.
Contact the company
What happened, in plain English
C.R. Bard is recalling urologist's trays that may have incorrect French size packaging. This could lead to improper use during medical procedures if the wrong size is used. Read more at govinfonow.com/recall/52159-c-r-bard-urologist-s-tray-recall-incorrect-french-size.
Source Summary by GovInfoNow · govinfonow.com/recall/52159-c-r-bard-urologist-s-tray-recall-incorrect-french-size · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2076-2025
Cite this page
“C.R. Bard Urologist's Tray Recall: Incorrect French Size Packaging.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52159-c-r-bard-urologist-s-tray-recall-incorrect-french-size. Based on FDA recall #Z-2076-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2076-2025%22&limit=1).
Why it’s dangerous
The packaging may contain the incorrect French size, which could lead to improper use during medical procedures. This might result in incorrect sizing for the urethra, potentially causing complications.
Who’s affected
Urologists and medical professionals who use the Bard Urologist's Tray for obstructed urethra procedures may be affected. Those using the specific lot numbers are most at risk.
How to tell if you have this one
Check for the lot number NGJX2513/UDI: 00801741000294 on the packaging. The product is sold under the reference number REF: 123400.
- Brand
C.R. Bard- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- 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.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2074-2025 | BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120; REF:21110 -Lot:JUJX0267/UDI:801741075506; REF:21112 -Lot:JUJX0258/UDI:801741075513; REF:21114 - Lots:JUJV0864 & JUJW5009/UDI:801741075520; REF:21120 -Lot:JUJY9171/UDI:801741075551 | — |
| Z-2075-2025 | BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316; REF:21312- Lot:JUJX0285 /UDI:801741075605; REF:21314- Lot:JUJX1147 /UDI:801741075612; REF: 21316- Lots:JUJY0895 & JUJX1148 /UDI:801741075629 | — |
| Z-2076-2025 | REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra; Lot # NGJX2513/UDI: 00801741000294 | 63 units |
What to do — step by step
Check Packaging
Look for the lot number NGJX2513/UDI: 00801741000294 on the packaging to identify affected units.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 39 states.
FDA 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…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 36 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2076-2025 (June 3, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2076-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.