FDAJuly 9, 2024device

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

What to do

FDA enforcement status: Ongoing

Brands named

covidien

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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