{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mercedita",
      "address_1": "Turpeaux Industrial Park Rd 1 km 123.4",
      "reason_for_recall": "As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013.  The affected products are sterile.",
      "address_2": "",
      "product_quantity": "2388",
      "code_info": "lot no.:  62141788  62194578  62284482  62284482N  61870886  61885906  61952556  61952557  62024629  62065277  62076884  62097070  62125314  62147327  62167372  62193417  62194579  62221879  62270707  62298289  62310428  62340081  62360302  61886895  61953169  62036899  62046493  62055999  62065278  62097073  62106807  62125315  62127736  62141792  62151830  62167373  62183148  62194580  62208755  62210445  62291930  62310435  62324097  62333971  62340080  62358910  62362926  61881190  61890332  61953170  61964733  62033228  62056001  62073507  62076886  62080036  62080037  62097076  62106804  62137224  62141789  62147328  62151832  62165198  62165199  62178286  62181429  62183150  62204531  62207225  62208757  62210446  62270709  62291929  62310430  62310432  62320165  62333970  62340077  62340078  62345388  62345389  62354664  62358904  62358905  61873652  61882614  61885902  61885904  61891301  61969293  62033229  62042592  62052831  62060680  62097077  62100687  62106802  62106803  62137225  62141790  62165201  62165202  62183149  62203186  62210447  62215710  62227046  62240749  62240750  62291931  62312488  62324096  62333976  62333978  62358908  62358909  61834957  61878471  61952559  61957434  61964735  62017573  62033230  62073508  62076888  62100688  62106805  62133327  62141791  62161482  62181430  62203187  62218181  62240751  62270711  62298290  62325574  62340079  61864115  62033231  62056002  62076889  62106806  62137226  62165203  62194581  62218180  62312489  62340082  62358903",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 71 consists of all product under product code: JDI and same usage:  Item no:\t  783401000\tVERSYS PRESS FIT LD/FX ST  783401100\tVERSYS PRESS FIT LD/FX SZ  783401200\tVERSYS PRESS FIT LD/FX SZ  783401300\tVERSYS PRESS FIT LD/FX SZ  783401400\tVERSYS PRESS FIT LD/FX SZ  783401500\tVERSYS PRESS FIT LD/FX SZ  783401600\tVERSYS PRESS FIT LD/FX SZ    For use in total or hemi hip arthroplasty",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1169-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72900",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20160111",
      "postal_code": "00715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}