Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq Technologies Inc. Due to It has been determined that the PINPOINT Operator's...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Novadaq Technologies Inc. directly.
Affected Products
PINPOINT Endoscopic Fluorescence Imaging System
Quantity: 110 units
Why Was This Recalled?
It has been determined that the PINPOINT Operator's Manual does not contain validated parameters for gravity-cycle autoclave sterilization of the PINPOINT laparoscopes and light guide cable in the reprocessing tray.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Novadaq Technologies Inc.
Novadaq Technologies Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report