Health Canada — Medical Devices · Canada · 2026-08-17 · Type I
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Reported risk: A communication is being issued to customers to provide information to be included in an upcoming change to the Instructions for Use. The additional information provides added details intended to reduce the risk of potential endoscope adherence and inability to spray powder.
Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.
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