{
  "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": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71272",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of AK, AL, AZ, CA, FL, GA, IL, IN, KS, MA, MI, MN, MO, NC, NY, OH, OK, PA, TX, UT, VA, WA, WI and countries of Canada, Australia, Japan, Taiwan, France, Germany, Spain, and Italy.",
      "recall_number": "Z-1699-2015",
      "product_description": "M/L Taper with Kinectiv¿ Technology.  prosthesis, hip, semi-constrained (metal uncemented acetabular component)    Product Usage:  Usage:  Total hip replacement for the following: severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, avascular necrosis of the femoral head, nonunion of previous fractures of the femur; congenital hip dysplasia, protrusio acetabuli, slipped capital femoral epiphysis; disability due to previous fusion; previously failed endoprostheses, and/or total hip components in the affected extremity and acute femoral neck fractures.",
      "product_quantity": "752",
      "reason_for_recall": "Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of M/L Taper with Kinectiv¿ femoral stems and modular necks due higher than allowed cytotoxicity levels found with the product.  Reasonable probability of adverse biological response and subsequent revision",
      "recall_initiation_date": "20150518",
      "center_classification_date": "20150608",
      "termination_date": "20160802",
      "report_date": "20150617",
      "code_info": "Product:   00771300500  Lots:   63006851  63006852  63024180  Product:  00771300600  Lots:  63024183  63024184  63024186  63024187  63024188  63024189  Product:  00771300700  Lots:  63024193  63024195  63024196  63024197  63024198  63024199  63024201  63024202  63024203  63024204  63024205  63024206  Product:  00771300900  Lots:  62927082  62927083  63024210  63024211  63024213  63024214  63024215  63024216  63024217  63024218  63024219  63024220  63024221  Product:  00771301000  Lots:  62938997  63024226  63024227  63024228  63024229  63024230  Product:  00771301100  Lots:  62885040  62905574  62998426  63024234  63024235  63024236  63024237  63024238  63024239  63024240  63024241  Product:  00771301200  Lots:  62927123  63024256  63024257  63024258  63024259  63024261  63024262  63024263  Product:  00771301300  Lots:  62885058  62939008  63024245  Product:  00784801400  Lot:  62924878  Product:  65771301100  Lot:  62939041"
    }
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}