{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Northfield",
      "address_1": "Three Lakes Drive",
      "reason_for_recall": "The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.",
      "address_2": "",
      "product_quantity": "4040 units",
      "code_info": "Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065",
      "center_classification_date": "20191218",
      "distribution_pattern": "USA - 2 consignees in PA only",
      "state": "IL",
      "product_description": "Anesthesia Pediatric Circuit 72\", Model DYNJAPF6057A",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medline Industries Inc",
      "recall_number": "Z-0698-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84283",
      "more_code_info": "",
      "recall_initiation_date": "20191030",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}