{
  "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": "2026-06-24",
    "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": "98484",
      "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": "Domestic distribution nationwide US. International distribution to Mexico and Panama.",
      "recall_number": "Z-1650-2026",
      "product_description": "Puracol and Puracol Plus Collagen Wound Dressings:    MSC8522\tDRESSING,COLLAGEN,PURACOL,STRL,2\" X 2\"  MSC8622EP\tDRESSING,COLLAGEN,PURACOL PLUS, 2X2.2\"",
      "product_quantity": "106,621 US; 2,350 OUS",
      "reason_for_recall": "Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension. In severe cases, septic shock may result.",
      "recall_initiation_date": "20260210",
      "center_classification_date": "20260326",
      "report_date": "20260401",
      "code_info": "MSC8522 - Puracol UDI-DI 10080196285860 (each) 40080196285861 (case) Lot P2090  MSC8622EP - Puracol Plus UDI-DI 10080196296804 (each) 40080196296805 (case) Lot PL2107",
      "more_code_info": ""
    }
  ]
}