{
  "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": "2026-07-08",
    "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": "98066",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states CA, CO, IL, KS, and MI.",
      "recall_number": "Z-0922-2026",
      "product_description": "FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048",
      "product_quantity": "53 units",
      "reason_for_recall": "The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.",
      "recall_initiation_date": "20251113",
      "center_classification_date": "20251212",
      "report_date": "20251224",
      "code_info": "DYNJ04048, UDI-DI: 10193489195248(each), 20193489195245(case), Lot Number: 2023112290",
      "more_code_info": ""
    }
  ]
}