{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89382",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "1450 E Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA and OH.",
      "recall_number": "Z-0548-2022",
      "product_description": "INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND",
      "product_quantity": "8 units (US)",
      "reason_for_recall": "The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw",
      "recall_initiation_date": "20220104",
      "center_classification_date": "20220201",
      "report_date": "20220209",
      "code_info": "UDI:  (01)10381780052234 (11)21101 (10)FVRG, Batch Numbers:  FTL9, FTLA, and FVRG"
    }
  ]
}