{
  "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": "00-5972-015-01 61777593  00-5972-018-02 4002192  00-5970-012-02 61878272  00-5970-013-02 61777576  00-5970-013-02 62135909  00-5970-014-02 11400192  00-5970-014-02 62122787  00-5970-014-02 62135920  00-5970-014-02 62132399  00-5970-014-02 62132399R  00-5970-014-02 62135921  00-5970-015-02 11002229  00-5970-015-02 61777581  00-5970-015-02 62135936  00-5970-016-02 61777583  00-5970-016-02 62128113  00-5970-017-01 11003049  00-5970-018-01 61758971  00-5970-018-01 11003323  00-5970-018-02 11003330  00-5970-018-02 11003322",
      "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": "CR PRECOAT FEM COMP SIZE BMR  CR PRECOAT FEM COMP SIZE C/R  CR PRECOAT FEM COMP SIZE D/R  CR PRECOAT FEM COMP SIZE E/R  CR PRECOAT FEM COMP SIZE F/R  CR PRECOAT FEM COMP SIZE G/L  CR PRECOAT FEM COMP SIZE H/L  CR PRECOAT FEM COMP SIZE H/R  CR POROUS FEM COMP SIZE E/L  CR POROUS FEM COMP SIZE H/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-1041-2018",
      "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"
    }
  ]
}