{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Englewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90753",
      "recalling_firm": "Paragon 28, Inc.",
      "address_1": "14445 Grasslands Dr",
      "address_2": "N/A",
      "postal_code": "80112-7062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, IN, LA, NJ, TX, WA, NY, MD, WI, OK, KY, MI, OH, CA, FL, KS, PA.",
      "recall_number": "Z-1776-2022",
      "product_description": "Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System",
      "product_quantity": "145",
      "reason_for_recall": "Suture anchor may break upon insertion, which could lead to potential debris in patient, and delays in surgery.",
      "recall_initiation_date": "20220713",
      "center_classification_date": "20220922",
      "report_date": "20220928",
      "code_info": "UDI-DI: 00889795114228, Lot: 5007499"
    }
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}