{
  "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": "94313",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "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, FL, KY, MS, TX, WA, WI, NC, VA, CA, SD, TN, GA, PA, TX.",
      "recall_number": "Z-1806-2024",
      "product_description": "namic CONVENIENCE KIT,   a) CAROTID MANIFOLD KIT, REF 60011045;   b) 3V MANIFOLD KIT ON WITH NAMIC DT & WASTE MANAGEMENT, REF 60070582;   c) LEFT HEART KIT, REF 60071822;   d) LEFT HEART KIT, REF 60080085;   e) CONVENIENCE KIT, REF 60100055;   f) CONVENIENCE KIT, REF 60101041;   g) CONVENIENCE KIT, REF 60120336;   h) LEFT HEART KIT, REF 60131446;   i) 3 VALVE MANIFOLD OFF KIT WITH SQUEEZE CONTRAST CONTROLLER AND PROTECTION  STATION, REF 60140798;   j) CONVENIENCE KIT, REF 60142592;   k) LEFT HEART KIT, REF 60183972;   l) FOUR VALVE MANIFOLD KIT, REF 60210209;   m) RIGHT HEART KIT, REF 60210862;   n) LEFT HEART KIT, REF 600705710;    o) CONVENIENCE KIT, REF 600803410;   p) TUBING KIT; REF 601322913;   q) LEFT HEART KIT, REF 60032582A",
      "product_quantity": "570 units",
      "reason_for_recall": "Products have a lack of sterility assurance.",
      "recall_initiation_date": "20240312",
      "center_classification_date": "20240510",
      "report_date": "20240522",
      "code_info": "a) UDI/DI 10193489040456, Lot Numbers:  0000113192;  b) UDI/DI 10193489044195, Lot Numbers:  0000113331;  c) UDI/DI 10193489044386, Lot Numbers:  0000112999;  d) UDI/DI 10193489044416, Lot Numbers:  0000113000;  d) UDI/DI 10193489044935, Lot Numbers:  0000113187;  e) UDI/DI  f) UDI/DI  g) UDI/DI  h) UDI/DI  i) UDI/DI  j) UDI/DI  k) UDI/DI  l) UDI/DI  m) UDI/DI  n) UDI/DI  o) UDI/DI  p) UDI/DI  q) UDI/DI"
    }
  ]
}