{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Waukegan",
      "address_1": "1170 S Northpoint Blvd",
      "reason_for_recall": "One of the cases of product might not have been sterilized.",
      "address_2": "",
      "product_quantity": "6/5-kit cases",
      "code_info": "Lot 17YM5936, Exp. 04/30/2019",
      "center_classification_date": "20180706",
      "distribution_pattern": "The product was distributed to UT.",
      "state": "IL",
      "product_description": "BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.",
      "report_date": "20180718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medline Industries, Inc.",
      "recall_number": "Z-2378-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "80197",
      "termination_date": "20200722",
      "more_code_info": "",
      "recall_initiation_date": "20180112",
      "postal_code": "60085-6757",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}