{
  "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": [
    {
      "status": "Terminated",
      "city": "Stockton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73157",
      "recalling_firm": "PMBS, LLC",
      "address_1": "40 Milltown Rd",
      "address_2": "N/A",
      "postal_code": "08559-1303",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, GA, MN, NY, OH, OR SC, and TN",
      "recall_number": "Z-1266-2016",
      "product_description": "The S.C.O.R.E.S. Unit (self contained operating room equipment  sterilization unit)",
      "product_quantity": "58 units",
      "reason_for_recall": "Water retention issues.  Units with filters that remain wet after the sterilization may compromised sterility.",
      "recall_initiation_date": "20160113",
      "center_classification_date": "20160325",
      "termination_date": "20170927",
      "report_date": "20160406",
      "code_info": "ALL distributed S.C.O.R.E.S. units are affected."
    }
  ]
}