Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covideien McGRATH MAC Video Laryngoscope Recalled by Covidien Due to IFU update to address device's battery handling information.
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 Covidien directly.
Affected Products
Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly
Quantity: 68,093 devices
Why Was This Recalled?
IFU update to address device's battery handling information.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien
Covidien has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report