{
  "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 units total",
      "code_info": "Part Numbers: 42517600303, 42517600313, 42517600505, 42517600515, 42517600707, 42517600717, 42517600909, 42517600919, 42527600303, 42527600313, 42527600505, 42527600515, 42527600707, 42527600717, 42527600909, and  42527600919. Lot numbers: 62345370, 62402721, 62423922, 62424796, 62494665, 62563912, 62590524, 62696878, 62717331, 62347233, 62399612, 62428432, 62505575, 62563917, 62592279, 62692687, 62352330, 62416376, 62432157, 62490790, 62563913, 62590525, 62696881, 62357329, 62374803, 62412999, 62432797, 62490792, 62563911, 62654931, 62717334, 62357328, 62372411, 62407772, 62432794, 62463961, 62525489, 62563914, 62575756, 62702758, 62724743, 62358632, 62373739, 62405896, 62432154, 62463962, 62563916, 62656074, 62710626, 62432790, 62462267, 62572574, 62443455, 62456923, 62568289, 62357865, 62410790, 62423921, 62424804, 62500930, 62573363, 62695299, 62347240, 62399870, 62430403, 62504858, 62572571, 62692683, 62732165, 62357866, 62406970, 62432150, 62479624, 62573364, 62695293, 62351310, 62410788, 62435708, 62507548, 62569955, 62698727, 62358633, 62373740, 62410789, 62432796, 62465722, 62517280, 62581856, 62695873, 62363685, 62364505, 62407568, 62432152, 62463963, 62505999, 62572570, 62695889, 62710608, 62432792, 62499171, 62704629, 62445747, and 62497257.",
      "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 Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD +0MM; L CD +6MM; L EF +0MM;L EF +6MM;  L GH +0MM; L GH +6MM;  L J +0MM; L J +6MM; R CD +0MM; R CD +6MM; R EF +0MM; R EF +6MM; R GH +0MM;  R GH +6MM; R J +0MM; R J +6MM; and",
      "report_date": "20140910",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-2575-2014",
      "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"
    }
  ]
}