{
  "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:  42517600303, 42517600313, 42517600505, 42517600515, 42517600707, 42517600717, 42517600909, 42517600919, 42527600303, 42527600313, 42527600505, 42527600515, 42527600707, 42527600717, 42527600909, 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  62497257",
      "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  Tibial Articular Surface Provisional Bottom  Nonsterile  PSN A/S PROV L CD BOTTOM +0MM  PSN A/S PROV L CD BOTTOM +6MM  PSN A/S PROV L EF BOTTOM +0MM  PSN A/S PROV L EF BOTTOM +6MM  PSN A/S PROV L GH BOTTOM +0MM  PSN A/S PROV L GH BOTTOM +6MM  PSN A/S PROV L J BOTTOM +0MM  PSN A/S PROV L J BOTTOM +6MM  PSN A/S PROV R CD BOTTOM +0MM  PSN A/S PROV R CD BOTTOM +6MM  PSN A/S PROV R EF BOTTOM +0MM  PSN A/S PROV R EF BOTTOM +6MM  PSN A/S PROV R GH BOTTOM +0MM  PSN A/S PROV R GH BOTTOM +6MM  PSN A/S PROV R J BOTTOM +0MM  PSN A/S PROV R J BOTTOM +6MM",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-2300-2014",
      "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"
    }
  ]
}