{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tuttlingen",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90118",
      "recalling_firm": "Smith & Nephew Orthopaedics GmbH",
      "address_1": "Alemannenstr. 14",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and internationally to Canada, Australia.",
      "recall_number": "Z-1133-2022",
      "product_description": "INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left   INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right",
      "product_quantity": "17 units",
      "reason_for_recall": "Right nails were anodized, marked, and labelled as left nails and vice versa",
      "recall_initiation_date": "20220422",
      "center_classification_date": "20220525",
      "report_date": "20220601",
      "code_info": "Product number: 71676627 (DI: 00885556131633), Batch Number: 21LT56988; 71676628 (DI: 00885556040027), Batch number: 21LT56989",
      "more_code_info": ""
    }
  ]
}