Atrium Medical Corporation: Medical Device Recall in 2017 - (Recall #: Z-1207-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 23, 2016

Date Posted: February 22, 2017

Recall Number: Z-1207-2017

Event ID: 75707

Reason for Recall:

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

Status: Terminated

Product Quantity: 2933 cases (17598 units)

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated