{
  "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": "1,187 units",
      "code_info": "Catalog/lot numbers:     45-751019 - 1903045J2, 1903065J2, 1903085J2, 1904155J2, 1904175J2, 1904265J2, 1904295J2, 1905035J2, 1905085J2, 1905105K2, and 1905135J2;    45-751324 - 1903045J2, 1903155J2, 1903205J2, 1903225J2, 1904155J2, 1904225J2, 1904265J2, 1904295J2, 1905065J2, and 1905085J2;      45-751632 - 1903045J2,  1903065J2, 1903205J2, 1903225J2, 1904175J2, 1904265J2, 1904295J2, 1905035J2, 1905065J2, and 1905085J2;    45-752039 - 1903045J2, 1903205J2, 1904265J2, 1905035J2, and 1905065J2;    45-750407 - 1903045J2,  1903065J2, 1903085J2, 1903115J2, 1903155J2, 1904175J2, 1904175K2, 1904225J2, 1904245J2, 1904265J2,  and1904295J2      45-750511 - 1903045J2,  1903065J2, 1903085J2, 1903155J2, 1904175J2, 1904175K2, 1904225J2, 1904245J2, 1904265J2, 1904295J2;    45-750617 - 1903045J2, 1903065J2, 1903085J2, 1903155J2, 1904055J2, 1905035J2, 1905065J2, and 1905085J2;    45-750609 - 1903045J2, 1903065J2, 1903085J2, and 1904035J2;    45-750812 - 1903045J2,  1903085J2, 1905035J2, 1905065J2, and 1905085J2;    45-750824 - 1903045J2, 1903065J2, 1903155J2 ,1904055J2, 1905035J2, 1905065J2, and 1905085J2;    MV-AX50407CD -  1904015J9, 1904035J9, and 1904085J9;    MV-AX50511CD -  1904015J9, 1904035J9, and 1904055J9;    MV-AX50617CD - 1904015J9 and 1904035J9;     MV-AX50824CD - 1904015J9 and 1904035J9; and     MV-AX51019CD - 1905105J9.",
      "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 CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039, 45-750407, 45-750511, 45-750617, 45-750609, 45-750812, 45-750824, MV-AX50407CD, MV-AX50511CD, MV-AX50617CD, MV-AX50824CD, and MV-AX51019CD,  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-1225-2020",
      "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"
    }
  ]
}