FDA Device Intelligence
Home › Device types › CAI

Circuit, Breathing (W Connector, Adaptor, Y Piece)

FDA product code CAI · Class 1 · Anesthesiology

7,212
Registered devices
2,509
Adverse events
205
Recalls
184
510(k) clearances

Devices with this code

Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Portex — ICU MEDICAL, INC.N/A — GALEMED CORPORATIONMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Vital Signs™ — AIRLIFEAirTechniques — Baldus Sedation GmbH & Co. KGMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Portex — ICU MEDICAL, INC.Standard Breathing Circuit with Mouthpiece — MEDITERA TIBBI MALZEME SANAYI VE TICARET ANONIM SIRKETIHUDSON RCI — TELEFLEX INCORPORATEDCarina VPack NIV NovaS Fullf M — Drägerwerk AG & Co. KGaAVital Signs™ — AIRLIFEVital Signs™ — AIRLIFEMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Anesthesia Set Coax 230 — Drägerwerk AG & Co. KGaAMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Curaplex — TRI-ANIM HEALTH SERVICES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.

Recent recalls

DateFirmReason
2026-08-11Medline Industries, LPThe kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the
2026-06-12Medline Industries, LPThe kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in t
2026-05-28Medline Industries, LPKits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injec
2026-05-28Medline Industries, LPConvenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Co
2026-05-06Medline Industries, LPThe Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection
2026-04-10Medline Industries, LPMedline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, incl
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market
2026-02-16Medline Industries, LPKits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster

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.