Official recall record

HEALON EndoCoat PRO

Health Canada · 2026-08-06 · CanadaType II

Issuing authority: Health Canada
Alert date: 2026-08-06
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

Johnson & Johnson Surgical Vision, Inc. is issuing a voluntary recall notice for HEALON EndoCoat™ PRO to inform customers of reports involving difficulty with insertion of the ultra-thin 25g orange cannula. This notice is intended to communicate the potential risks 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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — official record →
Record last checked against the registry on 2026-08-16.

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