{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99507",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "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 AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.",
      "recall_number": "Z-3019-2026",
      "product_description": "Medline convenience kits labeled as:    1) FEMORAL PACK, Medline Kit SKU DYNJ909393A;   2) FEVAR, Medline Kit SKU DYNJ910295D.",
      "product_quantity": "71 kits",
      "reason_for_recall": "Kits contain a potentially contaminated component which were recalled by the manufacturer",
      "recall_initiation_date": "20260710",
      "center_classification_date": "20260826",
      "report_date": "20260902",
      "code_info": "1) Medline Kit SKU DYNJ909393A, UDI/DI  10195327613945 (each) 40195327613946 (case) Lot Number 25ILA297;  2) Medline Kit SKU DYNJ910295D, UDI/DI 10198459586477 (each) 40198459586478 (case), Lot Number 26CBT178."
    }
  ]
}