{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92286",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1670-2023",
      "product_description": "Smith&Nephew ENGAGE Cementless Partial Knee System, Porous Femoral components, Part Numbers:    a)  REF 1-10003-100 (SIZE 1 Right Medial);   b)\tREF 1-10003-110 (SIZE 1 Left Medial);   c)\tREF 1-10003-200 (SIZE 2-Right Medial);   d)\tREF 1-10003-210 (SIZE 2-Left Medial);   e)\tREF 1-10003-300 (SIZE 3- Right Medial);   f)\tREF 1-10003-310 (SIZE 3- Left Medial);   g)\tREF 1-10003-400 (SIZE 4- Right Medial);   h)\tREF 1-10003-410 (SIZE 4- Left Medial);   i)\tREF 1-10003-500 (SIZE 5- Right Medial);   j)\tREF 1-10003-510 (SIZE 5- Left Medial);   k)\tREF 1-10003-600 (SIZE 6- Right Medial);   l)\tREF 1-10003-610 (SIZE 6- Left Medial);   m)\tREF 1-10003-700 (SIZE 7- Right Medial);   n)\tREF 1-10003-710 (SIZE 7- Left Medial);   o)  REF 1-10003-800, (SIZE 8 - Right Medial);   p)  REF 1-10003-810, (SIZE 8 - Left Medial);   Unicondylar knee prothesis",
      "product_quantity": "1994 units",
      "reason_for_recall": "Recent complaint data indicates that the revision rate may be trending higher than corresponding similar  devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.",
      "recall_initiation_date": "20230502",
      "center_classification_date": "20230531",
      "report_date": "20230607",
      "code_info": "a) REF 1-10003-100, UDI/DI 00885556872925;  b) REF 1-10003-110, UDI/DI 00885556872932; c) REF 1-10003-200, UDI/DI 00885556872949;  d) REF 1-10003-210, UDI/DI 00885556872956;  e) REF 1-10003-300, UDI/DI 00885556872963;  f) REF 1-10003-310, UDI/DI 00885556872970;  g) REF 1-10003-400, UDI/DI 00885556872987;  h) REF 1-10003-410, UDI/DI 00885556872994;  i) REF 1-10003-500, UDI/DI  00885556873007;  j) REF 1-10003-510, UDI/DI 00885556873014;  k) REF 1-10003-600, UDI/DI 00885556873021;  l) REF 1-10003-610, UDI/DI 00885556873038; m) REF 1-10003-700, UDI/DI 00885556873045;  n) REF 1-10003-710, UDI/DI 00885556873052;  o)  REF 1-10003-800, UDI/DI 00885556873069;  p)  REF 1-10003-810,  UDI/DI 00885556873076;    ALL BATCHES"
    }
  ]
}