{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Irvine",
      "address_1": "2361 McGaw Ave",
      "reason_for_recall": "The sterile battery may contain particulates within the sterile package.",
      "address_2": "",
      "product_quantity": "1995 total",
      "code_info": "Lots 509567, K055R",
      "center_classification_date": "20160311",
      "distribution_pattern": "Distributed in FL.",
      "state": "CA",
      "product_description": "Battery Pack  KLS-SD-1000  Single  Models: KLS-BP-001  Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Pro-Dex Inc",
      "recall_number": "Z-1095-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73034",
      "termination_date": "20170721",
      "more_code_info": "",
      "recall_initiation_date": "20151223",
      "postal_code": "92614-5831",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}