{
  "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": "00-5930-040-01 61774223  00-5930-040-01 61780003  00-5930-040-01 61774226  00-5930-040-01 61774225  00-5930-040-01 11005139  00-5930-050-01 61774236  00-5930-050-01 11004031  00-5930-060-01 61774234  00-5930-070-02 61780002  00-5930-070-01 62139076  00-5930-080-02 61774216  00-5930-080-01 61774229  00-5930-080-01 61780004  00-5930-080-02 61785662  00-5930-080-02 61774215",
      "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": "PRCT MIS CR MOB PLT SZ 4 L¿  PRCT MIS CR MOB PLT SZ 5 L¿  PRCT MIS CR MOB PLT SZ 6 L¿  PRCT MIS CR MOB PLT SZ 7 L¿  PRCT MIS CR MOB PLT SZ 7 R¿  PRCT MIS CR MOB PLT SZ 8 L¿  PRCT MIS CR MOB PLT SZ 8 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-1051-2018",
      "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"
    }
  ]
}