FDA Device Intelligence
HomeDevice types › BRY

Cabinet, Table And Tray, Anesthesia

FDA product code BRY · Class 1 · Anesthesiology

246
Registered devices
97,982
Adverse events
99
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2026-04-30CareFusion 303, Inc.Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
2025-12-03CareFusion 303, Inc.Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
2025-11-20CareFusion 303, Inc.Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a

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