Medical device recalls Moderate risk

Atrium Medical Corporation recalls Maquet Express Dry Seal Suction Chest Drain, Single Collection w/AC Reference: 4000-100N Intended Use: To evacuate air…

Recall date
December 23, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1208-2017
FDA classification
Class II
Brand / firm
Atrium Medical Corporation
Sold / distributed
Worldwide Distribution - US (nationwide) and Internationally to Canada and Mexico

Why it was recalled

Chest drains manual vent valve located at the top of affected chest drains could potentially not re-seal after being depressed.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Maquet Express Dry Seal Suction Chest Drain, Single Collection w/AC Reference: 4000-100N Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and reinfusion of autologous blood from the patients pleural cavity or mediastinal area

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