{
  "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": "Laredo",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90689",
      "recalling_firm": "Medline Industries Inc.",
      "address_1": "12001 General Milton",
      "address_2": "N/A",
      "postal_code": "78045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the state of AL.",
      "recall_number": "Z-1683-2022",
      "product_description": "Medline CHEST TUBE REORDER NO: DYNJ36762A",
      "product_quantity": "300 kits",
      "reason_for_recall": "Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit",
      "recall_initiation_date": "20220721",
      "center_classification_date": "20220907",
      "report_date": "20220914",
      "code_info": "Model Number: DYNJ36762A UDI-DI Code (GTIN Insert/GTIN Case / Lot Number: (01)1019348989440/(01)40193489894401 / 21ILA164 (01)1019348989440/(01)40193489894401 / 21ILA986 (01)1019348989440/(01)40193489894401 / 21JLA315 (01)1019348989440/(01)40193489894401 / 21KLA005 (01)1019348989440/(01)40193489894401 / 21KLA162 (01)1019348989440/(01)40193489894401 / 21KLA629"
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}