{
  "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": "65-5952-013-05 61819644  65-5952-013-05 61855471  65-5952-013-05 11004433  65-5952-013-06 62056868  65-5952-014-05 61782591  65-5952-014-05 11003623  65-5952-014-05 61987912  65-5952-014-05 62104150  65-5952-014-06 61835232  65-5952-014-06 62038826  65-5952-014-06 62132128  65-5952-015-05 61782592  65-5952-015-05 61822359  65-5952-015-05 61857405  65-5952-015-05 11004436  65-5952-015-05 61939607  65-5952-015-05 62020177  65-5952-015-05 62046101  65-5952-015-05 62122758  65-5952-015-06 61805662  65-5952-015-06 11003505  65-5952-015-06 61848476  65-5952-015-06 11004261  65-5952-015-06 61921288  65-5952-015-06 61968654  65-5952-015-06 62001382  65-5952-015-06 62025672  65-5952-015-06 62074886  65-5952-015-06 62128161  65-5952-016-05 61801433  65-5952-016-05 61836563  65-5952-016-05 61857407  65-5952-016-05 11004258  65-5952-016-05 11004438  65-5952-016-05 61928636  65-5952-016-05 61951539  65-5952-016-05 62020178  65-5952-016-05 62056869  65-5952-016-05 62092424  65-5952-016-05 62139313  65-5952-016-06 61777547  65-5952-016-06 61822354  65-5952-016-06 61857408  65-5952-016-06 11004434  65-5952-016-06 61904112  65-5952-016-06 61939609  65-5952-016-06 62002454  65-5952-016-06 62020219  65-5952-016-06 62062056  65-5952-016-06 62104151  65-5952-017-05 61824510  65-5952-017-05 61893908  65-5952-017-05 61939612  65-5952-017-05 62005729  65-5952-017-05 62025675  65-5952-017-05 62086012  65-5952-017-05 62132131  65-5952-017-06 11003018  65-5952-017-06 61795937  65-5952-017-06 61822355  65-5952-017-06 11003671  65-5952-017-06 61861698  65-5952-017-06 61846121  65-5952-017-06 11004260  65-5952-017-06 61915980  65-5952-017-06 61987914  65-5952-017-06 62020182  65-5952-017-06 62038827  65-5952-017-06 62105368",
      "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-FLX POR HATCP FEM C-L MINUS  CR-FLX POR HATCP FEM C-R MINUS  CR-FLX POR HATCP FEM D-L MINUS  CR-FLX POR HATCP FEM D-R MINUS  CR-FLX POR HATCP FEM E-L MINUS  CR-FLX POR HATCP FEM E-R MINUS  CR-FLX POR HATCP FEM F-L MINUS  CR-FLX POR HATCP FEM F-R MINUS  CR-FLX POR HATCP FEM G-L MINUS  CR-FLX POR HATCP FEM G-R MINUS    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-1031-2018",
      "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"
    }
  ]
}