{
  "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": "Bethlehem",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96212",
      "recalling_firm": "Tyber Medical",
      "address_1": "83 S Commerce Way Ste 310",
      "address_2": "N/A",
      "postal_code": "18017-8934",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1223-2025",
      "product_description": "A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left  Intended forFixation of fractures of the distal tibia  Model/Catalog Number: 770715121",
      "product_quantity": "201 units",
      "reason_for_recall": "Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices",
      "recall_initiation_date": "20250121",
      "center_classification_date": "20250221",
      "report_date": "20250305",
      "code_info": "UDI-DI 00196449016013;  Lot Numbers 265816, 24064DF01, 263557, 24065DF04, 24059DF03, 24059DF02"
    }
  ]
}