Home › Device types › BSY
Catheters, Suction, Tracheobronchial
FDA product code BSY · Class 1 · Anesthesiology
1,801
Registered devices
3,487
Adverse events
89
Recalls
116
510(k) clearances
Devices with this code
Ballard* Multi-Access Port Closed Suction System — Avanos Medical, Inc.VYGON — VYGONAVANOS — Avanos Medical, Inc.Bard® Suction Catheter Two Eye, Whistle Tip With Control Vent — C. R. Bard, Inc.AMSure® Coiled Suction Catheter — AMSINO INTERNATIONAL, INC.Res-Q-Vac — REPRO MED SYSTEMS, INC.Suction Catheters, Disposable — Dynarex CorporationFLEXFORM LINE — H.S. HOSPITAL SERVICE SPAPortex — ICU MEDICAL, INC.AVANOS — Avanos Medical, Inc.Res-Q-Vac — REPRO MED SYSTEMS, INC.AirLife™ — AIRLIFEBallard* Multi-Access Port Closed Suction System — Avanos Medical, Inc.BALLARD™ — SUNMED, LLCDAR — Covidien LPBALLARD™ — SUNMED, LLCRes-Q-Vac — REPRO MED SYSTEMS, INC.Res-Q-Vac — REPRO MED SYSTEMS, INC.Ballard* Closed Suction System for Adults — Avanos Medical, Inc.BALLARD™ — SUNMED, LLCMedSource Suction Pump — MEDSOURCE INTERNATIONAL LLCDAR — Covidien LPBALLARD™ — SUNMED, LLCDAR — Covidien LP
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2025-03-19 | Avanos Medical, Inc. | Lack of sterility assurance for closed suction catheter systems |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
| 2023-11-15 | MEDLINE INDUSTRIES, LP - Northfield | Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irr |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
