Data Foundry

Medical device recalls 2025

Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit… — Class I medical device recall Z-1697-2025

Ongoing recall by Vyaire Medical, reported 2025-05-21, distributed nationwide. Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection

Recall numberZ-1697-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmVyaire Medical, Mettawa, IL, United States
Recall initiated2025-04-10
Classified2025-05-09
Reported by FDA2025-05-21
DistributedNationwide (US)
Countries outside the USBE, DE, ES, GB, IN, IT, NL, PL, QA, RO, SA, SI
Quantity1,895
UPC / GTIN / UDI-DI10190752145139, 10889483595862, 30889483595866, 50190752145137
Serial numbers0004240347, 0004240348, 0004252021, 0004253194, 0004253470, 0004255176, 0004260100, 0004262183, 0004262987, 0004263371, 0004292077, 0004300092, 0004301668
Model numbersAH165

Product

Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas between the patient and a ventilator.

Reason for recall

Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1697-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.