Bard Peripheral Vascular Inc - Product List
Bard Peripheral Vascular Inc product list for medical devices. Includes a comprehensive list of products with their corresponding model numbers and dates.
Lower-risk recall
The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy needle, and the length of the cannula may exceed the stated length on the label. As a result, the biopsy needle may not fit properly into the coaxial cannula, preventing access to the target tissue, which could lead to tissue injury, longer and repeat procedures.
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What happened, in plain English
Bard Peripheral Vascular Inc has a wide range of medical devices with model numbers and dates. The list includes products from various dates and model numbers, such as 0001467001(04/28/25), 0001468229(04/28/25), etc. The products are organized by date ranges and model numbers. Read more at govinfonow.com/recall/56914-bard-peripheral-vascular-inc-product-list.
Source Summary by GovInfoNow · govinfonow.com/recall/56914-bard-peripheral-vascular-inc-product-list · Updated August 10, 2026 · FDA enforcement record: FDA #Z-0643-2024
Cite this page
“Bard Peripheral Vascular Inc - Product List.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/56914-bard-peripheral-vascular-inc-product-list. Based on FDA recall #Z-0643-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0643-2024%22&limit=1).
Why it’s dangerous
The list of products is for informational purposes and does not contain any harmful or dangerous information. It is a standard product listing for medical devices.
Who’s affected
Medical professionals, healthcare providers, and patients using Bard Peripheral Vascular Inc products
How to tell if you have this one
Check the model numbers and dates to ensure compatibility with the intended use and regulatory compliance.
- Brand
Bard Peripheral Vascular Inc- Category
Medical device
What to do — step by step
1. Verify the model numbers and dates
Ensure that the model numbers and dates match the intended use and regulatory requirements for the medical device.
2. Check for regulatory compliance
Confirm that the products comply with relevant medical device regulations and standards.
3. Review the product specifications
Examine the product specifications to understand the intended use, materials, and performance characteristics.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 50 states.
FDA distribution: “Worldwide - US Nationwide distribution including in the states of PR, IL, MA, GA, KY, CA, TX, PA, IA, MN, NH, MD, FL, ID, IN, AL, VA, CO, WI, NY, NV, OK, OH, WA, MI, MS, AZ, HI, SD, NJ, NE, MT, NC, DC, CT, WY, UT, TN, LA, NM, SC, VT, MO,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, 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, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 2 months 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.
Questions people ask
What are the model numbers listed?
The model numbers listed include various product codes such as 0001467001, 0001468229, etc., each associated with a specific date.
Are these products safe for use?
Yes, these products are designed and manufactured to meet medical device safety standards.
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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-0643-2024 (November 8, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0643-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 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.