FDAMarch 1, 2023device

Express Mini 500 Dry Seal Chest Drain, Part Number 16400

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

The hazard

The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the Express Mini 500 Dry Seal Chest Drains do not provide sufficient precaution against draining the device for continued use. Additionally, the IFUs do not provide sufficient precaution or warning against the use of the device outside the healthcare setting.

What to do

FDA enforcement status: Ongoing

Brands named

atrium medicalatrium

UPCs

00650862164008

Recall history

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

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