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

Recall Z-1080-2017 — Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean dual chamber, in-line connectors and suction control stopcock (2 Patient Tubes) 2020-100 Ocean dual chamber with in-line connectors and no suction control stopcock (2 Patient Tubes) 2020-300 Ocean dual chamber with suction contr

U.S. FDA — Device Enforcement · United States · 2016-11-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1080-2017
Date of alert
2016-11-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Atrium Medical Corporation
Product category
device
Product type
Devices
Reported risk: Outer Packaging is not sterile
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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