{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87887",
      "recalling_firm": "Alphatec Spine, Inc.",
      "address_1": "1950 Camino Vida Roble",
      "address_2": "N/A",
      "postal_code": "92008-6505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of FL, CA, IL, OK, TX, CT, IN, NC, WA,  HI, ID, MA, SC, NM, and NY.",
      "recall_number": "Z-1818-2021",
      "product_description": "Atec Insignia Anterior Cervical Plate System, REF 136-0354 Insignia, ACP, 3-Level, 54 mm, Rx Only, Non-Sterile, UDI: (01)00190376268583",
      "product_quantity": "7 units",
      "reason_for_recall": "There is a potential for the screw blocking mechanism on the  anterior cervical plate system  to disassociate intraoperatively/postoperatively or unlock postoperatively.",
      "recall_initiation_date": "20210426",
      "center_classification_date": "20210607",
      "termination_date": "20221117",
      "report_date": "20210616",
      "code_info": "8609324R"
    }
  ]
}