{
  "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": "Rockaway",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92294",
      "recalling_firm": "Linkbio Corp.",
      "address_1": "101 Round Hill Dr Ste 7",
      "address_2": "N/A",
      "postal_code": "07866-1214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX",
      "recall_number": "Z-1674-2023",
      "product_description": "LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6  Tilastan, cemented.  Intended for primary and revision total knee replacement.  Item Number: 880-325/13",
      "product_quantity": "11 units",
      "reason_for_recall": "Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).",
      "recall_initiation_date": "20230425",
      "center_classification_date": "20230601",
      "report_date": "20230607",
      "code_info": "UDI-DI : 04026575258123 Lot Number: 1910003"
    }
  ]
}