{
  "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": "2026-04-29",
    "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": "98594",
      "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  in the state of Alabama, Florida, and Kansas.",
      "recall_number": "Z-1810-2026",
      "product_description": "LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.",
      "product_quantity": "5 units",
      "reason_for_recall": "The CORE Workstation may display an incorrect \"Planning Date \" when viewing cases on the \"Start Case\" menu screen.",
      "recall_initiation_date": "20260312",
      "center_classification_date": "20260410",
      "report_date": "20260422",
      "code_info": "Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected."
    }
  ]
}