{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Blue Ash",
      "address_1": "4700 Ashwood Dr Ste 445",
      "reason_for_recall": "A defect involving an occluded needle was discovered during a training exercise.",
      "address_2": "",
      "product_quantity": "3,565 units",
      "code_info": "NSN 6515-01-655-9514  Lot number - 190524J69  Expiration Date - May 24, 2026",
      "center_classification_date": "20200212",
      "distribution_pattern": "US (nationwide), and countries of: Europe, Australia and Hong Kong.",
      "state": "OH",
      "product_description": "PneumoDart, 14 ga x 3.25in., REF TM-317    A compact, sterile, device intended for the introduction into the body to facilitate the removal of air from the pleural cavity as a result of a tension pneumothorax condition.",
      "report_date": "20200219",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Tytek Medical Inc",
      "recall_number": "Z-0930-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84296",
      "termination_date": "20201001",
      "more_code_info": "",
      "recall_initiation_date": "20191115",
      "postal_code": "45241-2684",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}