{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99692",
      "recalling_firm": "Onkos Surgical, Inc.",
      "address_1": "77 E Halsey Rd",
      "address_2": "N/A",
      "postal_code": "07054-3714",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of North Carolina, and California.",
      "recall_number": "Z-0090-2027",
      "product_description": "Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left  REF PV-ACREC-04M",
      "product_quantity": "1 implant",
      "reason_for_recall": "Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.",
      "recall_initiation_date": "20260724",
      "center_classification_date": "20261006",
      "report_date": "20261014",
      "code_info": "UDI: B278PVACREC04M0-Lot# C26-0346; Case# C26-0346,"
    }
  ]
}