Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
2.5 mm LifePort Endotracheal Tube Adapters 10-pack Recalled by Bunnell, Inc. Due to Some adaptors, for use with high frequency ventilators,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bunnell, Inc. directly.
Affected Products
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit Kits, Catalog: 938
Quantity: 1606 Assemblies
Why Was This Recalled?
Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal ventilator performance, which may lead to hypercarbia, hypoxia, and gas trapping.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bunnell, Inc.
Bunnell, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report