{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sacramento",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75255",
      "recalling_firm": "Hand Biomechanics Lab Inc",
      "address_1": "77 Scripps Dr Ste 104",
      "address_2": "N/A",
      "postal_code": "95825-6209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0136-2017",
      "product_description": "Agee-WristJack¿ Fracture Reduction System;  Item number: CFD-147.  The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. This is a single use system used for a trauma related surgery    The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. The non-perishable sterile system is packaged in an inner then outer tray and shipped in a cardboard shelf box.    Orthopedic:The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures.",
      "product_quantity": "65 units",
      "reason_for_recall": "A number of Agee WristJack¿ Fracture Reduction Systems have been manufactured with a molded beam slightly larger than optimal. This may result in the surgeon experiencing difficulty fine-tuning the length (red) and radial/ulnar alignment (blue) adjustments on the device.",
      "recall_initiation_date": "20160914",
      "center_classification_date": "20161018",
      "termination_date": "20161115",
      "report_date": "20161026",
      "code_info": "Lot number: HBL-115-165, serial numbers 47460959 and 47460980;  Lot number: HBL-116-014 - all serial numbers;  Lot number : HBL-116-040 - 15 systems shipped prior to recall"
    }
  ]
}