{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Westborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98280",
      "recalling_firm": "Miach Orthopaedics",
      "address_1": "69 Milk St Ste 100",
      "address_2": "N/A",
      "postal_code": "01581-1224",
      "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 AK, CA, CO, CT, FL, GA, IL, MA, MD, ME, MI, MN, MO, NC, NJ, NY, OH, OR, TX, VA, WA, WI.",
      "recall_number": "Z-1220-2026",
      "product_description": "BEAR Implant. Model Number: 1000.",
      "product_quantity": "284 units",
      "reason_for_recall": "Incorrect expiration date on label that extends beyond the product's documented/approved shelf life.  With an incorrect expiration date, the UDI will also be incorrect.",
      "recall_initiation_date": "20251231",
      "center_classification_date": "20260129",
      "report_date": "20260204",
      "code_info": "Model Number: 1000. UDI Number: (01)00860002987804(17)260228(10)7011098. Lot Number: 7011098. Expiration Date: 02/28/2026."
    }
  ]
}