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Recall Observatory FDA recall evidence

Device product

Maquet Oasis Dry Suction Water Seal Chest Drain, Single Collection w/AC Reference: 3600-100 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

Z-1207-2017

December 23, 2016

Class II

Product summary

Firm
Atrium Medical Corporation
Event
Event 75707
Status
Terminated
Classification
Class II
Quantity
2933 cases (17598 units)
Official record key
device-enforcement:Z-1207-2017

Official wording

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

Code information: Lot Number: 242909, 242910, 242912, 242914, 242915

Distribution pattern: Worldwide Distribution - US (nationwide) and Internationally to Canada and Mexico

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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