{
  "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": "3415",
      "code_info": "lot no.:  61678184  61839111  61852988  61862260  61875843  61882261  61898918  61974385  61988314  62002243  62002244  62024181  62031621  62090117  62109252  62263147  61875838  61895890  61895891  61912706  62037827  61649744  61660679  61764382  61882257  61887223  61988311  61988312  61988313  62009735  62037784  62090119  62109257  62153293  62160886  62263160  62109261  61396164  61634704  61664774  61777417  61777418  61782841  61782843  61782845  61782848  61810565  61810566  61810567  61810568  61810569  61810570  61810571  61839106  61839107  61839108  61839109  61852999  61853001  61853002  61853005  61875839  61875854  61882265  61887219  61887220  61893994  61894002  61915563  61915564  61915565  61938456  61938457  61938458  61938459  61980692  61980694  61980696  61980698  61985662  61985665  61985670  61985676  62009730  62009731  62009732  62009734  62017442  62017443  62017444  62024184  62024185  62024186  62031633  62038976  62038977  62038978  62090115  62097349  62097351  62097353  62120586  62120587  62120589  62120590  62120593  62134879  62134889  62134890  62150227  62150230  62150231  62153290  62153291  62153292  62160882  62160884  62193769  62193770  62193771  62204429  62204430  62204431  62204432  62204433  62263150  62263153  62263156  62263158  61649748  61782622  61782623  61782839  61810563  61810564  61839110  61852991  61852993  61875841  61875849  61882258  61887216  61887217  61898919  61985648  61985652  61985656  62002245  62002246  62002247  62009728  62009729  62024182  62024183  62031630  62090118  62118596  62134877  62150234",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 20 consists of all prod oct under  poduct code: KTT and same usage:  Item no:\t  47116201900\tCOMPRESSION SCREW 1/2IN  47116202300\tCOMPRESSION SCREW 1-1/2IN  47116202200\tCOMPRESSION SCREW 1-1/4IN  47116202400\tCOMPRESSION SCREW 1-3/4IN  47116202100\tCOMPRESSION SCREW 1IN  47116202000\tCOMPRESSION SCREW 3/4IN    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1118-2016",
      "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"
    }
  ]
}