Medical devicesUpdated Jan 3, 2026Bard Peripheral Vascular, Inc.Official source

    IMPRA® Carboflo™ Flex recall in Canada: missing material

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    In plain language

    This recall involves IMPRA® Carboflo™ Flex Carbon-Lined medical devices sold in Canada. It's being recalled because some units are missing a reinforcement material. Contact the manufacturer for more information if you have this product.

    What to do

    • Contact the manufacturer for additional information.

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    Affected products

    • IMPRA® Carboflo™ Flex Carbon-Lined

      Model: F5010C

      Lot: VTHV0076

    Why this matters

    Performance issue due to missing material

    Do I have this product?

    This recall only applies to specific products. Follow the steps below to check.

    1. 1

      Check the product name

      Make sure your product name matches one of the affected products listed above.

    2. 2

      Check the lot number

      Lot numbers identify specific production batches.

      Affected lots: VTHV0076

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: F5010C

    If your product matches one or more of the details above, it may be affected by this recall.

    If your product does not match these details, it is not affected by this recall.

    When in doubt, always check the official notice.

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    Frequently Asked Questions

    Why was this product recalled?

    Performance issue due to missing material

    What should consumers do?

    Contact the manufacturer for additional information.

    Where was the product sold?

    This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.

    Is there a health risk?

    Yes, there may be a health risk. Performance issue due to missing material

    When was this product recalled?

    This product was recalled on March 13, 2025.

    Is the Bard Peripheral Vascular, Inc. brand affected by this recall?

    Yes, Bard Peripheral Vascular, Inc. products are affected by this recall. This recall involves IMPRA® Carboflo™ Flex Carbon-Lined medical devices sold in Canada. It's being recalled because some units are missing a reinforcement material. Contact the manufacturer for more information if you have this product.