{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 8
    }
  },
  "results": [
    {
      "cfres_id": "194710",
      "product_res_number": "Z-1470-2022",
      "event_date_initiated": "2022-06-06",
      "event_date_created": "2022-07-27",
      "recall_status": "Open, Classified",
      "res_event_number": "90516",
      "product_code": "OEZ",
      "product_description": "Medline Convenience kits labeled as follows:  a. BEDSIDE PICC CDS, Model Number CDS984642, b. VASCULAR CDS, Model Number DYNJ902880J, c. VASCULAR CDS, Model Number DYNJ902880K, d. OPEN HEART A & B, Model Number DYNJ904831F, e. OPEN HEART MHS, Model Number DYNJ905394A, f. OPEN HEART MHS, Model Number DYNJ905394B, g. OPEN HEART WPH, Model Number DYNJ908168\nModel/Catalog Number: Model Numbers:  a.  CDS984642, b.  DYNJ902880J, c.  DYNJ902880K, d.  DYNJ904831F, e.  DYNJ905394A, f.  DYNJ905394B, g.  DYNJ908168\nProduct Description: convenience kits labeled as follows:",
      "code_info": "a. Model Number CDS984642, Lot codes:  19JBB553\nb. Model Number DYNJ902880J, Lot codes:  21FBR331, 21HBD394, 21IBP835, 21KBM214, 21DBE158\nc.  Model Number DYNJ902880K, Lot codes:  22BBD964, 21KBV788, 21LBN478\ne.  Model Number DYNJ904831F, Lot codes:  22DBT300, 22DBU172, 22BBO313, 21JBX260, 21KBO308\nf.  Model Number DYNJ905394A, Lot codes:  21HBJ840, 21IBU071, 21JBY922, 21DBS569, 21FBA011\ng.  Model Number DYNJ905394B, Lot codes:  22ABM646\nh.  Model Number DYNJ908168, Lot codes:  22EBB265",
      "firm_fei_number": "3000717925",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - SPT",
      "address_1": "1170 S Northpoint Blvd",
      "city": "Waukegan",
      "state": "IL",
      "postal_code": "60085-6757",
      "additional_info_contact": "Kassandra Cotner\n866-775-6072",
      "reason_for_recall": "Kits contain leaking bottles of isopropyl alcohol",
      "root_cause_description": "Under Investigation by firm",
      "action": "The firm's consignees were notified by US mail on 06/06/2022 and  instructed to destroy any affected kits on hand in accordance with their local and state regulations.",
      "product_quantity": "1960",
      "distribution_pattern": "US Nationwide distribution.",
      "openfda": {
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        ],
        "device_name": "Cardiovascular Procedure Kit",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.1200",
        "device_class": "2"
      }
    }
  ]
}