{
  "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": "Port Huron",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89605",
      "recalling_firm": "BioPro, Inc.",
      "address_1": "2929 Lapeer Rd",
      "address_2": "",
      "postal_code": "48060-2558",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CT, KY, NM, PA, TN, and SD.",
      "recall_number": "Z-0687-2022",
      "product_description": "Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036",
      "product_quantity": "",
      "reason_for_recall": "There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.",
      "recall_initiation_date": "20220201",
      "center_classification_date": "20220228",
      "termination_date": "20240228",
      "report_date": "20220309",
      "code_info": "Lot Number: 127603, 125590; UDI: 00810012480246",
      "more_code_info": ""
    }
  ]
}