FDA Device Intelligence
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Drain, Tee (Water Trap)

FDA product code BYH · Class 1 · Anesthesiology

144
Registered devices
39
Adverse events
2
Recalls
22
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2004-07-12Medex IncThe non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex.
2004-07-12Medex IncThe non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex.

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