{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98721",
      "recalling_firm": "Centinel Spine, Inc.",
      "address_1": "900 Airport Rd Ste 3b",
      "address_2": "",
      "postal_code": "19380-3416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, GA, LA, MO, NY, TN, TX.",
      "recall_number": "Z-2051-2026",
      "product_description": "Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6.    Total cervical disc replacement.",
      "product_quantity": "30 units",
      "reason_for_recall": "Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.",
      "recall_initiation_date": "20260320",
      "center_classification_date": "20260501",
      "report_date": "20260513",
      "code_info": "Model Number: PDSXL6; UDI-DI: 00843193113986; Lot Number: 2026-0027",
      "more_code_info": ""
    }
  ]
}