{
  "meta": {
    "disclaimer": "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. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Merrimack",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93149",
      "recalling_firm": "Atrium Medical Corporation",
      "address_1": "40 Continental Blvd",
      "address_2": "N/A",
      "postal_code": "03054-4332",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Algeria, Australia, Austria,  Bahrain, Belgium, Brazil, Brunei Darussalam, Canada, Chile, China, Czech Republic Ecuador, Egypt, Finland, France, Germany, Hong Kong, Iceland, Indonesia, Ireland, Israel,  Italy, Jordan, Korea, Republic of Kuwait, Latvia, Lithuania, Luxembourg, Malaysia,  Malta, Mauritius, Mexico, Montenegro, Netherlands, New Zealand, Norway, Pakistan,  Peru, Poland, Portugal, Puerto Rico, Qatar, Russian Federation, Saudi Arabia, Singapore,  Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan Province of China, Thailand Tunisia, Ukraine, United Arab Emirates, United Kingdom, Uruguay.",
      "recall_number": "Z-0317-2024",
      "product_description": "Oasis Dry Suction Water Seal Chest Drains (Oasis):  (1)3600-100 DRAIN, OASIS SINGLE W/AC;  (2)3612-100 DRAIN, OASIS PEDI A/C;  (3)3650-100 DRAIN, OASIS BRU W/AC;",
      "product_quantity": "471037 cases US; 638 case OUS",
      "reason_for_recall": "Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of  catheter(s) and patient tube connections with single collection chamber chest drains",
      "recall_initiation_date": "20230918",
      "center_classification_date": "20231116",
      "report_date": "20231122",
      "code_info": "UDI-DI:  (1)3600-100 DRAIN, OASIS SINGLE W/AC 20650862110016; (2)3612-100 DRAIN, OASIS PEDI A/C 20650862111013; (3) 3650-100 DRAIN, OASIS BRU W/AC 20650862113017  All lots within labeled product expiry Manufacturing Dates: Any product manufactured on and after July 21, 2020 Distribution Dates: Any product shipped on and after August 6, 2020"
    }
  ]
}