{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gurnee",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88984",
      "recalling_firm": "Ohio Medical Corporation",
      "address_1": "1111 Lakeside Dr",
      "address_2": "N/A",
      "postal_code": "60031-2489",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide, including PR.  There was government and foreign distribution.  There was no military distribution.",
      "recall_number": "Z-0482-2022",
      "product_description": "Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.",
      "product_quantity": "649 portable suction pumps and replacement pumps",
      "reason_for_recall": "Increase in premature device failures",
      "recall_initiation_date": "20211116",
      "center_classification_date": "20220111",
      "report_date": "20220119",
      "code_info": "Shipped between March 2019 and February 2021."
    }
  ]
}