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Recall Observatory FDA recall evidence

Device product

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.

Z-1993-2021

May 14, 2021

Class II

Product summary

Firm
Smiths Medical ASD Inc.
Event
Event 87983
Status
Terminated
Classification
Class II
Quantity
40 units
Official record key
device-enforcement:Z-1993-2021

Official wording

Reason: 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.

Code information: Lot Number 4072715

Distribution pattern: US Nationwide distribution in the states of PA, MI, MD, FL.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    incorrectly labeled