Home › Device types › BZA
Connector, Airway (Extension)
FDA product code BZA · Class 1 · Anesthesiology
1,093
Registered devices
473
Adverse events
38
Recalls
94
510(k) clearances
Devices with this code
DS 7-45 Bronchoscope Swivel — INSTRUMENTATION INDUSTRIES, INCORPORATEDAirLife™ — AIRLIFEDAR — Covidien LPAirLife™ — AIRLIFEConnector M34X1.5, 9/16 — Drägerwerk AG & Co. KGaABE 106 Adult Adapter with Vent — INSTRUMENTATION INDUSTRIES, INCORPORATEDMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.AincA® — ANESTHESIA ASSOCIATES, INC.AincA® — ANESTHESIA ASSOCIATES, INC.Hose kit adult, Aquapor — Drägerwerk AG & Co. KGaAHUDSON RCI — TELEFLEX INCORPORATEDFLEX CONNECTOR — King Systems Corporationn.a. — VBM Medizintechnik GmbHOxygen Connector — SUNSET HEALTHCARE SOLUTIONS, INC.CONNECTOR 22M - 22M, WITH MDI INSERT — Intersurgical IncorporatedOxygen Connector — SUNSET HEALTHCARE SOLUTIONS, INC.Right Angled Connector — VBM Medizintechnik GmbHIRMA™ Airway Adapter — MASIMO CORPORATIONNomoLine-O™ LH Pediatric Nasal/Oral CO2 Cannula 4m — MASIMO CORPORATIONNomoLine-O LH Adult Nasal CO2 Cannula with O2 — MASIMO CORPORATIONHUDSON RCI — TELEFLEX INCORPORATEDVital Signs™ — AirLife Finland OyAdaptors/Connectors — WESTMED, INC.HUDSON RCI — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-10 | Draeger, Inc. | Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts. |
| 2025-11-10 | Draeger, Inc. | Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts. |
| 2025-11-10 | Draeger, Inc. | Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts. |
| 2025-11-10 | Draeger, Inc. | Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts. |
| 2024-09-27 | Westmed, Inc. | Due to connector within the circuit flex extender not meeting specifications resulting in a low connection force and as a result, the connector may leak or disc |
| 2024-07-18 | Smiths Medical ASD Inc. | Uncertainty in the seal integrity of the sterile packaging. |
| 2023-04-05 | Smiths Medical ASD Inc. | DuraLife devices instructions for cleaning and sterilization have been determined to be inadequate. Specifically, for the DuraLife product, the IFU does not pro |
| 2023-04-05 | Smiths Medical ASD Inc. | DuraLife devices instructions for cleaning and sterilization have been determined to be inadequate. Specifically, for the DuraLife product, the IFU does not pro |
| 2023-04-05 | Smiths Medical ASD Inc. | DuraLife devices instructions for cleaning and sterilization have been determined to be inadequate. Specifically, for the DuraLife product, the IFU does not pro |
| 2019-08-15 | Bioseal Corporation | The reported stress crack in the port of the swivel elbow where the flip cap is inserted could result in leakage from the breathing system resulting in the pres |
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