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Cannula, Nasal, Oxygen
FDA product code CAT · Class 1 · Anesthesiology
1,827
Registered devices
1,767
Adverse events
6
Recalls
42
510(k) clearances
Devices with this code
NomoLine-O™ LH Adult Nasal/Oral CO2 Cannula 4m — MASIMO CORPORATIONResponsive Respiratory — RESPONSIVE RESPIRATORY, INC.DRIVEMEDICAL — Drive Devilbiss HealthcareHUDSON RCI — TELEFLEX INCORPORATEDNomoLine-O™ LH Adult Nasal/Oral CO2 Cannula with O2 4m — MASIMO CORPORATIONHUDSON RCI — TELEFLEX INCORPORATEDAdult Nasal Cannula, Large — Telesair, Inc.Medline — MEDLINE INDUSTRIES, INC.AirLife™ — AIRLIFEResp-O2 Nasal Oxygen Cannula Cushion Tip with Ultra Soft Ear Foam — Dynarex CorporationHUDSON RCI — MEDLINE INDUSTRIES, INC.n/a — SALTER LABSComfort Soft Plus™ FloEasy — WESTMED, INC.Ultima Oral + Nasal Cannula + Filter — Braebon Medical CorporationComfort Soft Plus CO2 Sampling Nasal Cannula — WESTMED, INC.AirLife™ — AIRLIFEO2 Cannula — SALTER LABSN/A — SALTER LABSn/a — SALTER LABSNatus — GCMEDICA ENTERPRISE LTD. (WUXI)MEDLINE — MEDLINE INDUSTRIES, INC.HUDSON RCI — TELEFLEX INCORPORATEDResp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Foam — Dynarex CorporationN/A — SALTER LABS
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2018-07-06 | Smiths Medical ASD Inc. | "Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured. |
| 2017-05-09 | Teleflex Medical | Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device. |
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