FDA Device Intelligence
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Needle, Emergency Airway

FDA product code BWC · Class 2 · Anesthesiology

11
Registered devices
22
Adverse events
2
Recalls
14
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2019-11-15Tytek Medical IncA defect involving an occluded needle was discovered during a training exercise.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.