{
  "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": "Telford",
      "address_1": "3135 Quarry Rd",
      "reason_for_recall": "Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply Units where the drive screw in the motor unit broke and the lift arm fell down approximately 60 cm (23.6 inches).",
      "address_2": "",
      "product_quantity": "139",
      "code_info": "Catalog numbers:MZ00614, MZ01038, MZ02190, MZ02254, and MZ02332",
      "center_classification_date": "20131114",
      "distribution_pattern": "Worldwide distribution: US (Nationwide)and in the country of Canada. (note: the ceiling supply units are not classified as a medical device by Health Canada).",
      "state": "PA",
      "product_description": "Draeger Movita 603x/DVE 803x Ceiling Supply Unit.  It is intended for use in operating theaters and intensive care",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Draeger Medical, Inc.",
      "recall_number": "Z-0282-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66537",
      "termination_date": "20140903",
      "more_code_info": "",
      "recall_initiation_date": "20130930",
      "postal_code": "18969-1042",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}