{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.",
      "address_2": "",
      "product_quantity": "13,227 in total",
      "code_info": "00-5994-013-91 61758275  00-5994-013-92 61758283  00-5994-014-92 61768114  00-5994-014-92 11004374  00-5994-014-92 11004966  00-5994-014-92 11006826  00-5994-015-91 11003022  00-5994-015-92 61771825  00-5994-015-92 61771822  00-5994-015-92 61771828  00-5994-015-92 61771826  00-5994-015-92 61771827  00-5994-016-91 61768099  00-5994-016-91 61771829  00-5994-016-91 11005670  00-5994-016-92 61768104  00-5994-016-92 61771832",
      "center_classification_date": "20180314",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.",
      "state": "IN",
      "product_description": "LCCK FEM IMPLANT SZ C-L  LCCK FEM IMPLANT SZ C-R  LCCK FEM IMPLANT SZ D-R  LCCK FEM IMPLANT SZ E-L  LCCK FEM IMPLANT SZ E-R  LCCK FEM IMPLANT SZ F-L  LCCK FEM IMPLANT SZ F-R    This device is indicated for patients with severe knee pain and disability",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1037-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78706",
      "termination_date": "20200402",
      "more_code_info": "",
      "recall_initiation_date": "20171129",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}