RecallGuide.ca
    Medical devices••Updated Jan 19, 2026•Aesculap AG•Official source

    Aesculap medical devices recall in Canada: Unlicensed import

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    In plain language

    This recall involves various Aesculap medical devices, including Endoscopy Trocars and Cannulas, imported into Canada. They are being recalled because they were imported without the appropriate license from Health Canada. No immediate action is required by end users as the devices are safe and effective.

    What to do

    • No immediate action is required by end users.
    • Contact the manufacturer if you need more information.

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    Affected products

    • Endoscopy Trocar

      Model: EJ824P, EJ826P, EK082P, EK084P, EK085P, EK090R, EK091R, EK093P, EK094P, EK097R, EK148SU, EK149SU, EK150SU, EK159SU, EK160SU, EK169SU, EK170SU, EK390R, EK397R

      Lot: Not applicable.

    • Susi Mosquito Forceps

      Model: BH111SU

      Lot: Not applicable.

    • Cannula, Suction/Irrigation

      Model: ER874R, ER876, OL168R, OL177R

      Lot: Not applicable.

    • Suction Tube

      Model: PG028R, SR550R, SR551R

      Lot: Not applicable.

    • Tube Set System

      Model: GA391, GA391SU

      Lot: Not applicable.

    • Bipolar Coag. Forceps

      Model: GK560R, GK580R, GK801R

      Lot: Not applicable.

    • Minop Trend Optic

      Model: PE487A, PE507A

      Lot: Not applicable.

    • Hi-Line Burr Diamond

      Model: GD763R, GD796R

      Lot: Not applicable.

    • Hi-Line Rosen Burr

      Model: GD742R, GD748R, GD811R, GD813R

      Lot: Not applicable.

    • Cannula, Suction

      Model: FH605SU, PG036SU

      Lot: Not applicable.

    • Handle, Suction

      Model: GF768R, GF966R

      Lot: Not applicable.

    • Minop Invent Trocar 30

      Model: FH620R

      Lot: Not applicable.

    • Silicone Brain Spatula

      Model: FF484R

      Lot: Not applicable.

    • Avm Micro Clip

      Model: FE902K, FE903K, FE904K, FE905K, FE908K, FE912K, FE913K, FE914K, FE915K

      Lot: Not applicable.

    • Minop Trocar

      Model: FF397R, FF398R, FF399R

      Lot: Not applicable.

    • Castroviejo Caliper

      Model: OB792R

      Lot: Not applicable.

    • Aesculap Yasargil Titanium Aneurysm Clip - Permanent

      Model: FT728D, FT780D, FT790D, FT792D

      Lot: Not applicable.

    • Spray Nozzle For GD450R/GD455R/GD465

      Model: GD460R

      Lot: Not applicable.

    • Wire Saw D

      Model: FH405, FH413, FH414, FH415

      Lot: Not applicable.

    • Cannula, Suction, Zoellner

      Model: GF772R, GF773R, GF774R

      Lot: Not applicable.

    • Hi-Line Lindemann Cutter

      Model: GD721R, GD724R

      Lot: Not applicable.

    • Antifogging Soln.Sterile F.Endoscopes

      Model: JG910

      Lot: Not applicable.

    • Uterine Cannula Leech-Wilkinson

      Model: ER871R, ER873R

      Lot: Not applicable.

    • Forceps Waugh Insul

      Model: GK016R

      Lot: Not applicable.

    • Silicone Ring With Needle

      Model: PL595SU

      Lot: Not applicable.

    • Cannula, Suction, Frazier

      Model: OP362R

      Lot: Not applicable.

    • Paediscope

      Model: FF373R, FF374R, FF378R

      Lot: Not applicable.

    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: Not applicable.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: BH111SU, EJ824P, EJ826P, EK082P, EK084P, EK085P, EK090R, EK091R, EK093P, EK094P, EK097R, EK148SU, EK149SU, EK150SU, EK159SU, EK160SU, EK169SU, EK170SU, EK390R, EK397R, ER871R, ER873R, ER874R, ER876, FE902K, FE903K, FE904K, FE905K, FE908K, FE912K, FE913K, FE914K, FE915K, FF373R, FF374R, FF378R, FF397R, FF398R, FF399R, FF484R, FH405, FH413, FH414, FH415, FH605SU, FH620R, FT728D, FT780D, FT790D, FT792D, GA391, GA391SU, GD460R, GD721R, GD724R, GD742R, GD748R, GD763R, GD796R, GD811R, GD813R, GF768R, GF772R, GF773R, GF774R, GF966R, GK016R, GK560R, GK580R, GK801R, JG910, OB792R, OL168R, OL177R, OP362R, PE487A, PE507A, PG028R, PG036SU, PL595SU, SR550R, SR551R

    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 Aesculap medical devices, including Endoscopy Trocars and Cannulas, imported into Canada. They are being recalled because they were imported without the appropriate license from Health Canada. No immediate action is required by end users as the devices are safe and effective.

    What should consumers do?

    No immediate action is required by end users. Contact the manufacturer if you need more 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?

    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 January 15, 2026.

    Is the Aesculap AG brand affected by this recall?

    Yes, Aesculap AG products are affected by this recall. This recall involves various Aesculap medical devices, including Endoscopy Trocars and Cannulas, imported into Canada. They are being recalled because they were imported without the appropriate license from Health Canada. No immediate action is required by end users as the devices are safe and effective.