{
  "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": "95852",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of UAE, and Canada.",
      "recall_number": "Z-0780-2025",
      "product_description": "Medline custom medical procedure kits labeled as:    1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476;   2) DIEP FLAP, REF DYNJ910120",
      "product_quantity": "74 units",
      "reason_for_recall": "Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.",
      "recall_initiation_date": "20241121",
      "center_classification_date": "20241230",
      "report_date": "20250108",
      "code_info": "1) REF DYNJ69476,  UDI/DI 10193489947786 (EA) 40193489947787 (CS), Lot Numbers:  21HDB296;   2) REF DYNJ910120, UDI/DI 10195327589202 (EA) 40195327589203 (CS), Lot Numbers:   24CMH776.",
      "more_code_info": ""
    }
  ]
}