{
  "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": "Reports of breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). The Persona primary knee surgical technique has been updated. This field action correction is to ensure that all distributors and users of this instrument are aware of the enhanced surgical techniques.",
      "address_2": "",
      "product_quantity": "77,737 total units",
      "code_info": "Part Numbers: 42517000410, 42517000510, 42517000610, 42517000710, 42527000410, 42527000510, 42527000610, and 42527000710.  Lot numbers: 62024975, 62043546, 62144792, 62152725, 62165538, 62187318, 62337961, 62372407, 62386776, 62397159, 62405917, 62456263, 62499170, 62551386, 62565051, 62568272, 62572572, 62663168, 62691384, 62707494, 62717346, 62020920, 62144793, 62156313, 62165539, 62184228, 62353932, 62356176, 62385100, 62420242, 62468277, 62538412, 62564340, 62611088, 62612263, 62690056, 62702295, 62717337, 62736078, 62024976, 62054776, 62147232, 62177243, 62187319, 62187320, 62359057, 62364955, 62391222, 62414006, 62461233, 62558583, 62564345, 62608889, 62638657, 62646286, 62702749, 62724348, 62394279, 62443397, 62487490, 62492802, 62506001, 62563915, 62568271, 62704633, 62055686, 62144796, 62161537, 62162597, 62256286, 62351297, 62356578, 62385099, 62404282, 62424802, 62455897, 62538392, 62565037, 62595855, 62611083, 62663162, 62680121, 62686205, 62695286, 62724347, 62724744, 62019863, 62156317, 62165548, 62168386, 62184268, 62256288, 62344258, 62356586, 62391232, 62391233, 62455892, 62504877, 62551337, 62564335, 62597816, 62638685, 62646284, 62695878, 62036673, 62138318, 62149715, 62189326, 62189327, 62356593, 62377738, 62391236, 62420225, 62461232, 62564360, 62564361, 62595865, 62611086, 62680120, 62690951, 62710615, 62761109, 62394280, 62428338, 62444959, 62500931, and 62568278.",
      "center_classification_date": "20140904",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY; and countries of: AUSTRALIA, INDIA, JAPAN, KOREA, SINGAPORE, AUSTRIA, BELGIUM, FRANCE, GERMANY, ISRAEL, ITALY, LUXEMBOURG, NETHERLANDS, SAUDI ARABIA, SOUTH AFRICA, SPAIN, SWITZERLAND, UNITED KINGDOM, and UNITED ARAB EMIRATES.",
      "state": "IN",
      "product_description": "PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional with the following: Left Size 3-9 CD Top; Left Size 3-11 EF Top; Left Size 7-12 GH Top; Left Size 9-12 J Top; Left Size 3-9 CD Top; Left Size 3-11 EF Top; Right Size 7-12 GH Top; and Right Size 9-12 J Top.",
      "report_date": "20140910",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-2577-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68878",
      "termination_date": "20150127",
      "more_code_info": "",
      "recall_initiation_date": "20140807",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}