{
  "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-1377-2022",
      "product_description": "Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No #15-2814/04).  orthopedic prosthesis.",
      "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   04026575316281 (Small)  04026575316298 (Medium)  04026575316304 (Large)    Serial/Lot Numbers:  210420/0762  210426/0311  210426/0363  210426/0364  210426/0374  210504/2485  210504/2552  210504/2564  210504/2566  210510/2845  210510/2846  210602/0215  210602/0265  210602/0266  210602/1068  210602/2717  210602/2721  210602/2733  210602/2769  210629/0893  210629/0919  210629/0929  210629/0967  210629/0969  210629/1046  210629/1051  210629/1054  210629/2750  210802/0663  210802/0771  210802/0841  210907/2316  210907/2317  210913/0613  210913/0622  210913/0762  210913/0797  210913/0801  210913/0809  210913/2167  211025/0391  211025/2541  211025/2543  211025/2563  211102/0426  211102/0431  211115/0220  211115/1948  211115/2111",
      "more_code_info": ""
    }
  ]
}