{
  "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": "Norderstedt",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90477",
      "recalling_firm": "Waldemar Link GmbH & Co. KG (Mfg Site)",
      "address_1": "Oststr. 4-10",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution to AL, CA, FL, GA, IL, IN, KS, MI, MN, NV, NY, OH, TN, TX, WA.  Foreign distribution to Algeria  Argentina  Australia  Austria  Belgium  Bulgaria  Canada  China  Colombia  Denmark  Ecuador  Estonia  Finland  France  Germany  Great Britain  Greece  Hungary  India  Indonesia  Israel  Italy  Latvia  Libya  Lithuania  Mexico  Netherlands  Norway  Pakistan  Peru  Philippines  Poland  Romania  Saudi Arabia  Slovakia  Slovenia  Spain  Sudan  Sweden  Switzerland  Thailand  Turkey  Ukraine  United Arab Emirates  Uruguy  Vietnam",
      "recall_number": "Z-1379-2022",
      "product_description": "Tibial Component.  orthopedic prosthesis. Model Nos:    Small, W\t16-2817/02                    Medium, W\t16-2817/05                    Large, W\t16-2817/07",
      "product_quantity": "3785",
      "reason_for_recall": "There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.",
      "recall_initiation_date": "20220524",
      "center_classification_date": "20220712",
      "report_date": "20220720",
      "code_info": "UDI-DI:    04026575359202 Small, W;  04026575359219 Medium, W;  04026575359226 Large, W;      Serial/Lot Numbers:  201002/1683  211025/1543  210202/0275  210302/0308  210314/1872  201002/1687",
      "more_code_info": ""
    }
  ]
}