{
  "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": "2026-08-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lebanon",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99315",
      "recalling_firm": "Permobil Inc",
      "address_1": "300 Duke Dr",
      "address_2": "N/A",
      "postal_code": "37090-8115",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN,  KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CAN.",
      "recall_number": "Z-2795-2026",
      "product_description": "Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock  REF:120031, Model version 3",
      "product_quantity": "140 units",
      "reason_for_recall": "This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,",
      "recall_initiation_date": "20240229",
      "center_classification_date": "20260724",
      "report_date": "20260805",
      "code_info": "All Units operating with firmware version 1.26.2/UDI:(01)17330818345674"
    }
  ]
}