The Recall Desk
HighFDA (Devices)·Z-0445-2026·Announced 2025-11-19

[pending] Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I;

Pending LLM rewrite. Source: FDA_DEVICE Z-0445-2026.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.

The recalled product

Product
Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I; LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D
Manufacturer
Medline Industries, LP

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • ENT DYNJ909128I UDI-DI 40198459333355 (case)
  • 10198459333354 (ea) Lots 25GBO685
  • LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D UDI-DI 40198459055301 (case)
  • 10198459055300 (ea) Lots 25GBN602

Distribution

Distributed nationwide across the United States.