{
  "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": "00-5790-020-00  00-5790-021-00  00-5790-022-00  00-5790-023-00  00-5790-024-00  00-5790-025-00  00-5790-026-00  00-5790-027-00  00-5790-028-00  00-5790-029-00  00-5790-030-00  00-5790-031-00    00-5790-020-00 61855504  00-5790-020-00 11004267  00-5790-020-00 61933229  00-5790-020-00 61915949  00-5790-020-00 11005144  00-5790-020-00 61949771  00-5790-020-00 62062057  00-5790-020-00 77001776  00-5790-022-00 61788933  00-5790-022-00 61810168  00-5790-022-00 61831670  00-5790-022-00 61894364  00-5790-022-00 11004689  00-5790-022-00 61910487  00-5790-022-00 61932359  00-5790-022-00 11004850  00-5790-022-00 61939861  00-5790-022-00 61958404  00-5790-022-00 61993535  00-5790-022-00 61987879  00-5790-022-00 62041075  00-5790-022-00 62074833  00-5790-022-00 11006797  00-5790-022-00 77001778  00-5790-024-00 61788934  00-5790-024-00 61805631  00-5790-024-00 61822278  00-5790-024-00 61928510  00-5790-024-00 61952565  00-5790-024-00 62025572  00-5790-024-00 62054459  00-5790-024-00 62068114  00-5790-024-00 62080645  00-5790-024-00 62105235  00-5790-024-00 77001780  00-5790-024-00 62110658  00-5790-026-00 61777601  00-5790-026-00 61815430  00-5790-026-00 61824552  00-5790-026-00 61952567  00-5790-026-00 62005615  00-5790-026-00 11006199  00-5790-026-00 62062058  00-5790-026-00 62086067  00-5790-026-00 77001782  00-5790-028-00 61831671  00-5790-028-00 62062059  00-5790-028-00 11006735  00-5790-028-00 77001784  00-5790-030-00 61881087  00-5790-030-00 61968455  00-5790-030-00 77001786  00-5790-021-00 61933230  00-5790-021-00 11005163  00-5790-021-00 11005243  00-5790-021-00 62013359  00-5790-021-00 11006254  00-5790-021-00 62086803  00-5790-021-00 77001777  00-5790-023-00 11003416  00-5790-023-00 61795864  00-5790-023-00 11003680  00-5790-023-00 61810169  00-5790-023-00 11003843  00-5790-023-00 61889207  00-5790-023-00 61904081  00-5790-023-00 61933231  00-5790-023-00 61928509  00-5790-023-00 61949247  00-5790-023-00 61993546  00-5790-023-00 62020300  00-5790-023-00 62056497  00-5790-023-00 62074834  00-5790-023-00 77001779  00-5790-025-00 61777599  00-5790-025-00 61795865  00-5790-025-00 61822279  00-5790-025-00 61899451  00-5790-025-00 61928511  00-5790-025-00 61936678  00-5790-025-00 61952566  00-5790-025-00 11005169  00-5790-025-00 62000808  00-5790-025-00 62020301  00-5790-025-00 62056498  00-5790-025-00 62074835  00-5790-025-00 62080646  00-5790-025-00 11006839  00-5790-025-00 62104129  00-5790-025-00 77001781  00-5790-027-00 61782626  00-5790-027-00 61824553  00-5790-027-00 61921258  00-5790-027-00 61952568  00-5790-027-00 62045723  00-5790-027-00 62068115  00-5790-027-00 62092386  00-5790-027-00 77001783  00-5790-029-00 61805632  00-5790-029-00 62005616  00-5790-029-00 77001785  00-5790-031-00 62002487  00-5790-031-00 77001787",
      "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": "FEM PRC LT M/RT L SML           FEM PRC RT M/LT L SML           FEM PRC LT M/RT L SML+          FEM PRC RT M/LT L SML+          FEM PRC LT M/RT L REG           FEM PRC RT M/LT L REG           FEM PRC LT M/RT L REG+          FEM PRC RT M/LT L REG+          FEM PRC LT M/RT L LGE           FEM PRC RT M/LT L LGE           FEM PRC LT M/RT L LGE+          FEM PRC RT M/LT L LGE+     \" 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-1055-2018",
      "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"
    }
  ]
}