RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Karl Storz Se & Co. KgOfficial source

    Karl Storz medical devices recall in Canada: labelling and packaging issue

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    In plain language

    This recall involves various Karl Storz flexible endoscopes sold in Canada. They are being recalled due to an issue with labelling and packaging regarding reprocessing instructions. Customers should stop using the endoscopes if they do not have access to appropriate sterilization methods and return them to Karl Storz.

    What to do

    • Stop using the product immediately if you cannot sterilize it as recommended.
    • Contact the manufacturer for additional information.
    • Return the endoscopes to Karl Storz as instructed.

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    Affected products

    • Flexible Digital Video Cystoscope

      Model: 11272VN, 11272VNU

      Lot: More than 10 numbers, contact manufacturer.

    • Flexible Video Cystoscope Hd-View

      Model: 11272VH-TL, 11272VHU-TL

      Lot: More than 10 numbers, contact manufacturer.

    • Broncho Fiberscope

      Model: 11005BC1

      Lot: More than 10 numbers, contact manufacturer.

    • Ureteroscope

      Model: 11278AC1, 11278AC2, 11278ACU1

      Lot: More than 10 numbers, contact manufacturer.

    • Flexible Video-Uretero-Renoscope Flex-Xc

      Model: 11278V/VU, 11278VA, 11278VSA, 11278VSE, 11278VSU, 11278VSUA, 11278VSUE, 11278VU, 11278VUA

      Lot: More than 10 numbers, contact manufacturer.

    • Flexible Cystoscope

      Model: 11272C1, 11272C2, 11272CU1, 11272V, 11272VA, 11272VU, 11272VUA, 11272VUE, 11272VUE-R

      Lot: More than 10 numbers, contact manufacturer.

    • Flexible Pediatric Cystoscope

      Model: 11274BCU1

      Lot: More than 10 numbers, contact manufacturer.

    • Rhin0-Laryngo Fiberscope

      Model: 11001RD1

      Lot: More than 10 numbers, contact manufacturer.

    • Flexible Uretero-Reno Fiberscope

      Model: 11278A2, 11278AU1

      Lot: More than 10 numbers, contact manufacturer.

    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: More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 11001RD1, 11005BC1, 11272C1, 11272C2, 11272CU1, 11272V, 11272VA, 11272VH-TL, 11272VHU-TL, 11272VN, 11272VNU, 11272VU, 11272VUA, 11272VUE, 11272VUE-R, 11274BCU1, 11278A2, 11278AC1, 11278AC2, 11278ACU1, 11278AU1, 11278V/VU, 11278VA, 11278VSA, 11278VSE, 11278VSU, 11278VSUA, 11278VSUE, 11278VU, 11278VUA

    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?

    This recall involves various Karl Storz flexible endoscopes sold in Canada. They are being recalled due to an issue with labelling and packaging regarding reprocessing instructions. Customers should stop using the endoscopes if they do not have access to appropriate sterilization methods and return them to Karl Storz.

    What should consumers do?

    Stop using the product immediately if you cannot sterilize it as recommended. Contact the manufacturer for additional information. Return the endoscopes to Karl Storz 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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on April 11, 2022.

    Is the Karl Storz Se & Co. Kg brand affected by this recall?

    Yes, Karl Storz Se & Co. Kg products are affected by this recall. This recall involves various Karl Storz flexible endoscopes sold in Canada. They are being recalled due to an issue with labelling and packaging regarding reprocessing instructions. Customers should stop using the endoscopes if they do not have access to appropriate sterilization methods and return them to Karl Storz.