Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0741-2014 — Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain Dual patient lines; Product Code: 3652-100. To evacuate air and/or fluid from the chest cavity or mediastinum.

U.S. FDA — Device Enforcement · United States · 2013-11-19 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0741-2014
Date of alert: 2013-11-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Atrium Medical Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10883097

Reported risk: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0741-2014 — Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain Dual patient lines; Product Code: 3652-100. To evacuate air and/or fluid from the chest cavity or mediastinum.

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