FDAFebruary 13, 2025device

Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary collapse.

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

UPCs

1501931501863315019315018640

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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