FDANovember 15, 2019device

PneumoDart, 14 ga x 3.25in., REF TM-317 A compact, sterile, device intended for the introduction into the body to facilitate the removal of air from the pleural cavity as a result of a tension pneumothorax condition.

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

The hazard

A defect involving an occluded needle was discovered during a training exercise.

What to do

FDA enforcement status: Terminated

Brands named

tytek medicaltytek

UPCs

6515016559514

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →