{
  "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": "Port Huron",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97605",
      "recalling_firm": "BioPro, Inc.",
      "address_1": "2929 Lapeer Rd",
      "address_2": "",
      "postal_code": "48060-2558",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Domestic distribution to Texas and Michigan.",
      "recall_number": "Z-0153-2026",
      "product_description": "BioPro Femoral Head     Product ID/Description  14089\tHEAD FEMORAL 28 SH LT  14090\tHEAD FEMORAL 28 MD LT  14091\tHEAD FEMORAL 28 LG LT  14094\tHEAD FEMORAL 32 SH LT  14095\tHEAD FEMORAL 32 MD LT  14096\tHEAD FEMORAL 32 LG LT",
      "product_quantity": "147 total",
      "reason_for_recall": "Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.",
      "recall_initiation_date": "20250909",
      "center_classification_date": "20251014",
      "report_date": "20251022",
      "code_info": "Product ID/UDI-DI  14089 M20914089 14090 M20914090 14091 M20914091 14094 M20914094 14095 M20914095 14096 M20914096  All lots, all serial numbers",
      "more_code_info": ""
    }
  ]
}