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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Atrium Medical Corporation: Chest drains have a missing o-ring

Agency Publication Date: June 29, 2015
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Affected Products

Product: Ocean Water Seal Chest Drain, Single Collection W/AC, P/N: 2002-000

Lot Number: 222511

Lot Numbers:
Number
Product: Ocean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100

Lot Number: 222945

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Number
Product: Oasis Dry Suction Water Seal Chest Drain, DRY SINGLE W/AC P/N: 3600-100

Lot Numbers: 222115, 222118, 222528

Lot Numbers:
Numbers
Product: EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N

Lot Number: 222516

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 71023
Status: Resolved
Manufacturer: Atrium Medical Corporation
Manufactured In: United States
Units Affected: 4 products (390 cases; 130 cases; 1170 cases; 390 cases)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.