{
  "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": "445 units",
      "code_info": "Catalog/lot numbers:     45-481015 - 19031155A;     45-481020 - 19031355E and 190424567;     45-481215 - 19031154K and 19041554Z;     45-481220 - 19051357G;     45-481515 - 19041554W and 19041556Q;     45-481520 - 19032053A;     45-482020 - 190320539 and 19040855Y;     45-482030 - 19040855X;     45-480202 - 19032054J and 190506581;     45-480204 - 19051357N;     45-480310 - 19031154N, 19031355G, 190401554, and 19050657X;     45-480302 - 19050657V and 19051357P;     45-480305 - 19031154L, 19031354G, 19031355F, 19042254K, 19042453J, 19050657W, and 19051357L;     45-480410 - 19031154G,19031155B, 19031354H, 19031355H, 19032054N, 190415553, 19042254L, and 19051357K;     45-480415 - 19041554V and 19050657U;     45-480420 - 190506582 and 19051357H;     45-480405 - 190424568;    45-480610 - 19041554Y, 19041556V, and 19051357J;     45-480615 - 19042254G;     45-480620 - 19031354J, 19041554X, and 19042453K;     45-480815 - 19040853U and 190415552;     45-480820 - 19031355J,19032053C, and 19032252U;     MV-AZ80520HL - 190401556, 190401566, and 19040554H;      MV-AZ80202HL - 190517542 and 190517566;      MV-AZ80204HL - 19051756C;     MV-AZ80305HL - 190517543;     MV-AZ80310HL - 190517544;     MV-AZ80410HL - 19040554J and 19040555X;     MV-AZ80420HL - 19050253Y, 19050254W, 190517545, and 190517569;     MV-AZ80620HL - 19050254V and 190517546;      MV-AZ80820HL - 19051756A; and     MV-AZ81020HL - 190517564.",
      "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 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-480610, 45-480615, 45-480620, 45-480815, 45-480820, MV-AZ80520HL, MV-AZ80202HL, MV-AZ80204HL, MV-AZ80305HL, MV-AZ80310HL, MV-AZ80410HL, MV-AZ80420HL, MV-AZ80620HL, MV-AZ80820HL, and MV-AZ81020HL, 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-1220-2020",
      "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"
    }
  ]
}