{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Englewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90436",
      "recalling_firm": "Paragon 28, Inc.",
      "address_1": "14445 Grasslands Dr",
      "address_2": "",
      "postal_code": "80112-7062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.",
      "recall_number": "Z-1468-2022",
      "product_description": "HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)",
      "product_quantity": "9 implants",
      "reason_for_recall": "Due to Titanium plasma coating not present implant.",
      "recall_initiation_date": "20220526",
      "center_classification_date": "20220727",
      "report_date": "20220803",
      "code_info": "Part Number: P40-002-0275-S UDI-DI Code: (01)00889795033987(17)270323(10)26010822202 Lot Number: 26010822202",
      "more_code_info": ""
    }
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}