{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "41816",
      "product_res_number": "Z-0109-06",
      "event_date_initiated": "2005-08-24",
      "event_date_posted": "2005-11-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-04-05",
      "res_event_number": "33361",
      "product_code": "MAY",
      "k_numbers": [
        "K955871"
      ],
      "product_description": "Citation AT Femoral Stem",
      "code_info": "Catalog #-- Description-- # of lots:  6265-2-102, Citation AT Left Hip Stem #2,  11 lots; 6265-2-103, Citation AT Left Hip Stem #3,  15 lots; 6265-2-104, Citation AT Left Hip Stem #4,  31 lots; 6265-2-105, Citaiton AT Left Hip Stem #5,  31 lots; 6265-2-112, Citation AT Left Hip Stem #2,    1 lot # P4GFD; 6265-2-113, Citation AT Left Hip Stem  #3,  49 lots; 6265-2-114, Citation AT Left Hip Stem  #4 , 27 lots; 6265-2-115, Citation AT Left Hip Stem  #5,  23 lots.",
      "firm_fei_number": "3003070421",
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "city": "Mahwah",
      "state": "NJ",
      "postal_code": "07430-2002",
      "additional_info_contact": "Dominick Cristofolo\n201-831 Ext. 5247",
      "reason_for_recall": "The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.",
      "root_cause_description": "Other",
      "action": "A urgent product recall notification was sent out to all hospitals on August 24, 2005, branches and agencies by first class mail.\nThe action is limited only to that product manufactured in the Stryker Ireland facility for the product families indicated.",
      "product_quantity": "207 units",
      "distribution_pattern": "nationwide",
      "openfda": {
        "k_number": [
          "K051844",
          "K123604",
          "K090103",
          "K110807"
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        ],
        "device_name": "Prosthesis,  Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish",
        "medical_specialty_description": "Orthopedic",
        "regulation_number": "888.3353",
        "device_class": "2"
      }
    }
  ]
}