{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "Customer complaints received for the presence of leaks",
      "address_2": "",
      "product_quantity": "8640 eaches",
      "code_info": "H16F16088",
      "center_classification_date": "20170119",
      "distribution_pattern": "US only",
      "state": "IL",
      "product_description": "APD Set with Cassette 3-Prong Peritoneal Dialysis Set    Indicated for use in the treatment of patients  with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD systems in clinical and home use settings.",
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      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corporation",
      "recall_number": "Z-1056-2017",
      "initial_firm_notification": "Letter",
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      "termination_date": "20170824",
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      "recall_initiation_date": "20161216",
      "postal_code": "60015-4625",
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