FDA Device Intelligence
HomeDevice types › BTS

Tube, Bronchial (W/Wo Connector)

FDA product code BTS · Class 2 · Anesthesiology

51
Registered devices
2,475
Adverse events
11
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21Teleflex, Inc.Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-02-28Teleflex MedicalThe product may fail to achieve seal of right lung due to the cuff inflating to one side

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