FDAMay 14, 2021device
PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit, REF 100/596/090 - Product Usage: intended for use in a controlled setting such as an Intensive Care Unit or operating room with the assistance of trained personnel.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
One lot number of a specific model of ULTRAperc Percutaneous Dilation Tracheostomy Kit, 9.0mm may have been incorrectly labeled as a 7.0mm ID kit.
What to do
FDA enforcement status: Terminated
Brands named
smiths medical asdsmithssmiths medical
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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