{
  "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": "Wheeling",
      "address_1": "241 W Palatine Rd",
      "reason_for_recall": "Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line",
      "address_2": "",
      "product_quantity": "180 units",
      "code_info": "Model Number IMKBMN-13R-6,  Lot Number LFD9",
      "center_classification_date": "20190207",
      "distribution_pattern": "Worldwide distribution - US Nationwide in the states of New Jersey,  and countries of Mexico and South Korea.",
      "state": "IL",
      "product_description": "J  Type Bone Marrow Needle  13ga x 6cm - Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.",
      "report_date": "20190213",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Angiotech (Manan Medical Products, Inc.)",
      "recall_number": "Z-0816-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81968",
      "termination_date": "20200823",
      "more_code_info": "",
      "recall_initiation_date": "20181218",
      "postal_code": "60090-5824",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}