{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Aliso Viejo",
      "address_1": "35 Enterprise",
      "reason_for_recall": "The devices may be missing the implant coil.",
      "address_2": "",
      "product_quantity": "19 units",
      "code_info": "Catalog/lot numbers:     45-651026 - 19030655Y, 19041556W, and 19051058A; and     45-652050 - 19030654Y and 19041556X.",
      "center_classification_date": "20200213",
      "distribution_pattern": "The devices were distributed to Maryland.  There was no direct military/government distribution.  Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.",
      "state": "CA",
      "product_description": "Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx.  The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.",
      "report_date": "20200219",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Microvention, Inc.",
      "recall_number": "Z-1224-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84585",
      "termination_date": "20210420",
      "more_code_info": "",
      "recall_initiation_date": "20191124",
      "postal_code": "92656-2601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}