{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.",
      "address_2": "",
      "product_quantity": "70,986 distribution events",
      "code_info": "Item Numbers:  42517000410  Lot Numbers:   62024975  62043546  62144792  62152725  62165538  62187318  62337961  62372407  62386776  62397159  62405917  62456263  62499170  62551386  62568272  62572572  62565051  62663168  62691384  62707494  62717346",
      "center_classification_date": "20140821",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including DC and Puerto Rico and the states of  AK, AL, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WY, and the countries of Australia, Canada, Germany, India, Japan, Korea, and Singapore.",
      "state": "IN",
      "product_description": "Persona (TM) The Personalized  Knee System  CR Tibial Articular Surface Provisional Top  Nonsterile    TASP CR L 3-9 CD TOP",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-2298-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68817",
      "termination_date": "20140911",
      "more_code_info": "",
      "recall_initiation_date": "20130610",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}