{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87530",
      "recalling_firm": "Centinel Spine, Inc.",
      "address_1": "900 Airport Rd Ste 3b",
      "address_2": "N/A",
      "postal_code": "19380-3416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, MD, DC, TN, GA, NC, PA, KY, NY, AZ, CO, OH, FL, MI.",
      "recall_number": "Z-1406-2021",
      "product_description": "Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following single-level discectomy for intractable symptomatic cervical disc disease (SCDD),   Part number: 09.820.055S",
      "product_quantity": "49 devices",
      "reason_for_recall": "Centinel Spine learned through five customer complaints that the product was missing the \"UP\" etching on the superior plate of the prodisc C device. Per the Surgical Technique, the \"UP\" is one of the methods used to indicate the direction in which the surgeon should place the prodisc C into intradiscal space. There are also \"UP\" indications in the packaging and on instrumentation as additional guides to help the surgeon properly implant the device that were present for the affected product.",
      "recall_initiation_date": "20210305",
      "center_classification_date": "20210409",
      "termination_date": "20210802",
      "report_date": "20210421",
      "code_info": "UDI  (01)00843193112842(17)241231(10)2020-0600  Lot number: 2020-0600"
    }
  ]
}