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Stimulator, Nerve, Battery-Powered

FDA product code BXN · Class 2 · Anesthesiology

113
Registered devices
31
Adverse events
5
Recalls
63
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-05-17B Braun Medical IncThe devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
2024-05-17B Braun Medical IncThe devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
2024-05-17B Braun Medical IncThe devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
2024-05-17B Braun Medical IncThe devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
2010-02-01Stryker Instruments Div. of Stryker CorporationDevice may malfunction and lead to ineffective stimulation, which could delay finding the nerve and the effects of the nerve block.

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