{
  "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": "392 units",
      "code_info": "Catalog/lot numbers:     45-451015 - 190410589;     45-451020- 19030456J,  19041056C, 19041756Y, 190422549, and 190422573;    45-451215 -190410569;     45-451220 -19040853N;     45-451230 -19041554R;     45-451520 -19030654N,  190408565, 190410588, and 190422572;    45-451530 -19030456L, 190408569, 19041056A, 190415571, 19041756Z, 190417599, 19042656G, and 19050254X;    45-452020 -19030456N, 19030654L, 19030655W, 19040856A, and 19041552H;    45-452030 - 19041058A,  19041554U, and 19042656H;    45-450410 - 19030456C, 19030655V, 19041058F, and 190422575;    45-450415 - 190422574;     45-450405 - 19030453C,  19030456B, and 19042254B;    45-450610 - 19030456E, 19030654W, 190410568, and 19041058E;    45-450615 - 19030456F, 190401568, 19041058C, and 19041556Y;    45-450620 - 19030453J and 19030655N;    45-450815 - 19030456G, 19030654U, 19050253U, and 19050254Z;    45-450820 - 19030453K,19030456H, 19030654R, 19030655G, 19030655H, 19050253V, 19050254Y, 19050657T, and 19051058C; and      MV-AZ52030HD - 190405564.",
      "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, Helical HydroCoil Embolization System,  REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-AZ52030HD, 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-1223-2020",
      "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"
    }
  ]
}