{
  "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": "00-5842-012-02 61777606  00-5842-012-02 61774093  00-5842-013-01 61774095  00-5842-013-02 61777611  00-5842-014-01 11002921  00-5842-014-01 61777613  00-5842-014-02 61777615  00-5842-014-02 61777616  00-5842-015-01 61777617  00-5842-016-02 61756843",
      "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": "ZUK PRC FEM SZB RMED/LLAT¿  ZUK PRC FEM SZC LMED/RLAT¿  ZUK PRC FEM SZC RMED/LLAT¿  NGU PRC FEM SZD LMED/RLAT¿  ZUK PRC FEM SZD RMED/LLAT¿  ZUK PRC FEM SZE LMED/RLAT  ZUK PRC FEM SZF RMED/LLAT    \" These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. \" These devices are indicated for cemented use only. \" The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1054-2018",
      "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"
    }
  ]
}