[Recalled] Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F — Firm received multiple complaints of anesthesia circuit leaks due to cracks in… | FDA
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F |
|---|---|
| Brand / manufacturer | Medline Industries, LP |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0444-2026 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 10 October 2025 |
| EAN / barcode | 40198459055356 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.