Home › Device types › BZA
Connector, Airway (Extension)
FDA product code BZA · Class 1 · Anesthesiology
1,080
Registered devices
466
Adverse events
38
Recalls
94
510(k) clearances
Devices with this code
HUDSON RCI — TELEFLEX INCORPORATEDGaleMed — GaleMed Xiamen Co., Ltd.NomoLine-O™ LH Adult Nasal/Oral CO2 Cannula 4m — MASIMO CORPORATIONConnector M34X1.5, 9/16 — Drägerwerk AG & Co. KGaAHUDSON RCI — TELEFLEX INCORPORATEDNomoLine-O™ LH Adult Nasal/Oral CO2 Cannula with O2 4m — MASIMO CORPORATIONAincA® — ANESTHESIA ASSOCIATES, INC.CapnoTrak — Respironics Novametrix, LLCOxygen Connector — SUNSET HEALTHCARE SOLUTIONS, INC.CONNECTOR 22M - 22M, WITH MDI INSERT — Intersurgical IncorporatedAincA® — ANESTHESIA ASSOCIATES, INC.AincA® — ANESTHESIA ASSOCIATES, INC.AincA® — ANESTHESIA ASSOCIATES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.IRMA Airway Adapter — MASIMO CORPORATIONAincA® — ANESTHESIA ASSOCIATES, INC.HUDSON RCI — TELEFLEX INCORPORATEDBlueSet Ventilation (P/A) — Drägerwerk AG & Co. KGaAN/A — Intersurgical IncorporatedErgoStar CM 55 — Drägerwerk AG & Co. KGaAHUDSON RCI — TELEFLEX INCORPORATEDN/A — GaleMed Xiamen Co., Ltd.HUDSON RCI — MEDLINE INDUSTRIES, INC.n.a. — VBM Medizintechnik GmbH
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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