{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91968",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX.",
      "recall_number": "Z-1430-2023",
      "product_description": "Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and  ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only.  A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments.    Note: The CCR basket lid is also distributed with ME764 CCR Basket - Full System",
      "product_quantity": "ME754: 3 units; ME764: 22 units",
      "reason_for_recall": "Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct  GTIN # is 04046955299607.",
      "recall_initiation_date": "20230223",
      "center_classification_date": "20230425",
      "report_date": "20230503",
      "code_info": "GUIDID: 04046955299592 (Basket Lid)"
    }
  ]
}