FDA Device Intelligence
HomeDevice types › OFP

Anesthesia Breathing Circuit Kit (Adult & Pediatric)

FDA product code OFP · Class 1 · Anesthesiology

691
Registered devices
104
Adverse events
33
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-03-12Draeger, Inc.The potential for cracks forming in the breathing circuit hose.
2025-03-12Draeger, Inc.The potential for cracks forming in the breathing circuit hose.
2025-03-12Draeger, Inc.The potential for cracks forming in the breathing circuit hose.
2025-03-12Draeger, Inc.The potential for cracks forming in the breathing circuit hose.
2025-03-12Draeger, Inc.The potential for cracks forming in the breathing circuit hose.
2021-01-29Draeger Medical, Inc.Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the
2021-01-29Draeger Medical, Inc.Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the
2021-01-29Draeger Medical, Inc.Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the
2021-01-29Draeger Medical, Inc.Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the
2020-11-11Intersurgical IncThe device was assembled with the incorrect exhalation port which can cause gas leakage.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.