{
  "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": "Mundelein",
      "address_1": "750 Tower Rd",
      "reason_for_recall": "Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.",
      "address_2": "Suite A",
      "product_quantity": "81 units",
      "code_info": "Item: 346VA;   Lot Numbers: D3, E3, F3",
      "center_classification_date": "20130921",
      "distribution_pattern": "Distributed in the states of FL, TX, and VA.",
      "state": "IL",
      "product_description": "ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description   5mm Atraumatic Grasper S/A, Standard; Non-sterile; Manufactured by Endoplus; 750 Tower Rd., Suite A, Mundelein, IL 60060 USA.    Intended for grasping, dissecting, retraction, clamping in conjunction with the laparoscopic during laparoscopic surgery.",
      "report_date": "20131002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Endoplus, Inc.",
      "recall_number": "Z-2264-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66063",
      "termination_date": "20160208",
      "recall_initiation_date": "20130715",
      "postal_code": "60060-3818",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}