Medical devicesUpdated Jan 3, 2026Sunmed Holdings, LLC Dba Ventlab, LLCOfficial source

    Airflow™, SafeSpot™ and Horizon™ Resuscitators

    Share:

    In plain language

    This recall involves Airflow, SafeSpot, and Horizon Resuscitators sold in Canada. They are being recalled due to device compatibility issues when using certain accessories. Stop using the product and contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for additional information.

    Get alerts for recalls like this

    Get email alerts when new recalls affect products in this category.

    Categories (optional)

    No spam. Unsubscribe anytime. We only email when there's a relevant recall.

    Affected products

    • Airflow™ Small Child Resuscitator (AF4000 Series)

      Model: AF4100MBP

      Lot: All lots

    • SafeSpot™ Infant Resuscitator (SS3200 Series)

      Model: SS3200MB, SS3200MB-2

      Lot: All lots

    • Airflow™ Pediatric Resuscitator (AF2000 Series)

      Model: AF2100MB, AF2140MB-PW

      Lot: All lots

    • Airflow™ Infant Resuscitator (AF3000 Series)

      Model: AF3100MB, AF3100MB-M1, AF3100MBP

      Lot: All lots

    • Airflow™ Small Adult Resuscitator (AF5000 Series)

      Model: AF5100MB, AF5140MBS

      Lot: All lots

    • Horizon™ Adult Resuscitator

      Model: HZI9111

      Lot: All lots

    Why this matters

    Device compatibility issues

    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: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: AF2100MB, AF2140MB-PW, AF3100MB, AF3100MB-M1, AF3100MBP, AF4100MBP, AF5100MB, AF5140MBS, HZI9111, SS3200MB, SS3200MB-2

    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.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Device compatibility issues

    What should consumers do?

    Stop using the product immediately. 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. Device compatibility issues

    When was this product recalled?

    This product was recalled on February 7, 2024.

    Is the Sunmed Holdings, LLC Dba Ventlab, LLC brand affected by this recall?

    Yes, Sunmed Holdings, LLC Dba Ventlab, LLC products are affected by this recall. This recall involves Airflow, SafeSpot, and Horizon Resuscitators sold in Canada. They are being recalled due to device compatibility issues when using certain accessories. Stop using the product and contact the manufacturer for more information.