FDANovember 2, 2022device
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
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
bunnell
UPCs
106161200000341061612000008900616120000082
Recall history
No related federal recalls on record for this brand yet.
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