FDAOctober 5, 2020device

TyTek PneumoDart- Intended for introduction into the body to facilitate removal of air from the pleural cavity in patients with a tension pneumothorax Model Number: TM-317

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

The hazard

Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location

What to do

FDA enforcement status: Terminated

Brands named

tytek medicaltytek

UPCs

00855204008167

Recall history

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

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