{
  "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": "00-5950-012-02  00-5950-013-01  00-5950-013-02  00-5950-013-06  00-5950-014-01  00-5950-014-02  00-5950-014-05  00-5950-014-06  00-5950-015-01  00-5950-015-02  00-5950-015-05  00-5950-015-06  00-5950-016-01  00-5950-016-02  00-5950-016-05  00-5950-016-06  00-5950-017-01  00-5950-017-02  00-5950-017-05  00-5950-017-06",
      "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-FLEX PCT FEM B-R  CR-FLEX PCT FEM C-L  CR-FLEX PCT FEM C-R  CR-FLEX PCT FEM D-L  CR-FLEX PCT FEM D-R  CR-FLEX PCT FEM E-L  CR-FLEX PCT FEM E-R  CR-FLEX PCT FEM F-L  CR-FLEX PCT FEM F-R  CR-FLEX PCT FEM G-L  CR-FLEX PCT FEM G-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-1050-2018",
      "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"
    }
  ]
}