OFFICIAL-SOURCE RECALL · CANADA
HEALON EndoCoat PRO Recall: s associated with cannula insertion and provide
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
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Is your product affected?
- Brand
- See official notice
- Product
- HEALON EndoCoat PRO
- Manufacturer
- See official notice
- Serial number / range
- number
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
s associated with cannula insertion and provide additional clarification regarding insertion technique to support the safe and effective use of the product. This recall does not require removal or return of the product from the market. When used in accordance with the instructions provided in this notice, the product may continue to be used as intended. Additional information Details Original
Hazard
s associated with cannula insertion and provide additional clarification regarding insertion technique to support the safe and effective use of the product. This recall does not require removal or return of the product from the market. When used in accordance with the instructions provided in this notice, the product may continue to be used as intended. Additional information Details Original
Official recall notice
HEALON EndoCoat PRO
Agency: Health Canada
Official publication date: August 6, 2026
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