{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Southington",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96755",
      "recalling_firm": "Silex Medical, LLC",
      "address_1": "24 Robert Porter Rd Ste B",
      "address_2": "N/A",
      "postal_code": "06489-1158",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of Florida, North Dakota, Illinois, California, Texas, Virginia, Michigan, Connecticut, Oregon, Iowa, Mississippi, New Jersey, Idaho, West Virginia, Hawaii.",
      "recall_number": "Z-1898-2025",
      "product_description": "Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863050.",
      "product_quantity": "7 units",
      "reason_for_recall": "Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel.",
      "recall_initiation_date": "20240109",
      "center_classification_date": "20250602",
      "report_date": "20250611",
      "code_info": "Model/REF Number: 5863050. UDI-DI: B33158630500. Lot Number: M28186. Serial Numbers: 1051, 1052, 1053, 1054, 1055, 1056, 1057, 1058, 1059"
    }
  ]
}