{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Laurel",
      "address_1": "8880 Gorman Rd",
      "reason_for_recall": "Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patients.",
      "address_2": "",
      "product_quantity": "15 units",
      "code_info": "Serial Numbers:  QABS50026  QABR50066  QABR50068  QABR50133  QABS50023  QABR50102  QABR50103  QABR50064  QABR50065  QABR50067  QABS50070  QABS50069  QABR50275  QABS50027  QABR50274",
      "center_classification_date": "20140203",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including Puerto Rico and the countries of Uruguay, Venezuela, Albania, Algeria, Australia, Austria, Bahrain, Belarus, Belgium, Bolivia, Canada, Chile, China, Costa Rica, Cyprus, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Iraq, Ireland, Israel, Italy, Kazakhstan, Korea, Kuwait, Lithuania, Macedonia, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Nigeria, Norway, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, United Arab Emirates, and United Kingdom.",
      "state": "MD",
      "product_description": "Stand-Alone Resuscitation Unit, Bag and Mask, part number M1226444, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com***.    Provides the basic equipment required for pulmonary resuscitation of infants.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare",
      "recall_number": "Z-0914-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67225",
      "termination_date": "20150601",
      "more_code_info": "",
      "recall_initiation_date": "20131212",
      "postal_code": "20723-5800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}