Bard Peripheral Vascular Inc product list for medical devices. Includes a comprehensive list of products with their corresponding model numbers and dates.
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.
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.
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.
Medical professionals, healthcare providers, and patients using Bard Peripheral Vascular Inc products
Check the model numbers and dates to ensure compatibility with the intended use and regulatory compliance.
Ensure that the model numbers and dates match the intended use and regulatory requirements for the medical device.
Confirm that the products comply with relevant medical device regulations and standards.
Examine the product specifications to understand the intended use, materials, and performance characteristics.
Bard Peripheral Vascular Inc is a medical device manufacturer specializing in peripheral vascular products.
The model numbers listed include various product codes such as 0001467001, 0001468229, etc., each associated with a specific date.
Yes, these products are designed and manufactured to meet medical device safety standards.
We’ve drafted a message you can send Bard Peripheral Vascular Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-0643-2024 — Bard Peripheral Vascular Inc Bard Peripheral Vascular Inc Hello, I own a Bard Peripheral Vascular Inc that is covered by recall Z-0643-2024 from Bard Peripheral Vascular Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
