RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Endo GIAOfficial source

    Endo GIA Reload recall in Canada: serious injury risk

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    In plain language

    This recall involves various Endo GIA Reload surgical staplers sold in Canada. They are being recalled because a manufacturing defect could cause staples to not deploy, leading to serious injury or death. Stop using the product and follow the return steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model and lot numbers.
    • Return the product as instructed.

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    Affected products

    • Endo GIA Reload w/Tri-Staple Technology Med/Thick

      Model: EGIA45AMT, EGIA60AMT

      Lot: N7M0047KX, N7M0617KX, N7M1001KX, N8A0203KX

    • Endo GIA Curved Tip Reload w/Tri-Staple Technology Vascular/Medium

      Model: EGIA45CTAVM

      Lot: N7L1041KX, N8A0199KX

    • Endo GIA Curved Tip Reload w/Tri-Staple Technology Vascular

      Model: EGIA30CTAV, EGIA45CTAV

      Lot: N7L0818KX, N7L0819KX

    • Endo GIA Gray Articulating Reload Extra Thin/Vascular

      Model: EGIA45AV

      Lot: N7L0823KX, N8A0799KX

    Why this matters

    Serious injury or death due to stapler malfunction

    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: N7L0818KX, N7L0819KX, N7L0823KX, N8A0799KX, N7L1041KX, N8A0199KX, N7M0047KX, N7M0617KX, N7M1001KX, N8A0203KX

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: EGIA30CTAV, EGIA45AMT, EGIA45AV, EGIA45CTAV, EGIA45CTAVM, EGIA60AMT

    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?

    Serious injury or death due to stapler malfunction

    What should consumers do?

    Stop using the product immediately. Check model and lot numbers. Return the product as instructed.

    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. Serious injury or death due to stapler malfunction

    When was this product recalled?

    This product was recalled on June 6, 2018.

    Is the Endo GIA brand affected by this recall?

    Yes, Endo GIA products are affected by this recall. This recall involves various Endo GIA Reload surgical staplers sold in Canada. They are being recalled because a manufacturing defect could cause staples to not deploy, leading to serious injury or death. Stop using the product and follow the return steps in the official notice.