{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98399",
      "recalling_firm": "International Life Sciences",
      "address_1": "8601 Dunwoody Pl Ste 250",
      "address_2": "N/A",
      "postal_code": "30350-2513",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, OK, \tOR, PA, SD, TN, TX, UT, VA, WA, WI, WY and the countries of Australia, France, Germany, Italy, Japan, Korea, Spain, Switzerland, United Kingdom, United Arab Emirates, Slovenia.",
      "recall_number": "Z-1556-2026",
      "product_description": "Artelon FLEXBAND  TWIST .12         Ref: TW012  3.85x17mm HEX Anchor (Qty 2)  5.0x17mm HEX Anchor (Qty 1)  0.5x12cm FLEXBAND (Qty 1)",
      "product_quantity": "N/A",
      "reason_for_recall": "Augmentation devices failed bacterial endotoxin testing.",
      "recall_initiation_date": "20260206",
      "center_classification_date": "20260311",
      "report_date": "20260318",
      "code_info": "Lot: RK29976/GTIN: 00850003396248"
    }
  ]
}