{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Gurnee",
      "address_1": "1111 Lakeside Dr",
      "reason_for_recall": "Final quality control testing was not completed before the devices were distributed..",
      "address_2": "",
      "product_quantity": "11 units",
      "code_info": "UDI 08688250002085; Catalog Numbers 8702-1251-908, 8701-1251-901, 8705-1251-907, 8701-1251-908, 8705-1251-901; Lot Number ISU177359; Device Unit Numbers JGGW24156, JGGW24193, JGGW24157,  JGGW24161 ,JGGW24167, JGGW24169, JGGW24175, JGGW24188, JGGW24189, JGGW24198, JGGW24160",
      "center_classification_date": "20180710",
      "distribution_pattern": "US Nationwide Distribution in the states of NC, IN, TN, LA,, FL MI, IL.",
      "state": "IL",
      "product_description": "Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU)    Product  Usage:  The vacuum regulator is intended to be used in a medical facility as a means to evacuate media (i.e. fluids) from the body.",
      "report_date": "20180718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ohio Medical Corporation",
      "recall_number": "Z-2410-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "80294",
      "termination_date": "20200716",
      "more_code_info": "",
      "recall_initiation_date": "20180312",
      "postal_code": "60031-2489",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}