{
  "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": "M/L Taper Hip Prosthesis and M/L Taper Hip Prosthesis with Kinectiv Technology manufactured prior to October 2015 are being recalled due to the potential for black residue to be observed within the polyethylene bag containing the implant. The black residue is a combination of the titanium plasma spray used to create the porous surface of the implant and polyethylene bag containing the implant. The recalling firm states the residue is biocompatible. Risks include delay of surgery while locating a replacement device, and surgical intervention due to wear caused by debris.",
      "address_2": "",
      "product_quantity": "510",
      "code_info": "61349197  61690629  61721526  61781828  62010553  62118873  62130040  62201735  62258067  62275219  62356222  62361475  62484285  62496087  62546976  62559966  62578405  62616562  62634733  62652960  62700955  62733912  62798024  62808130  62808133  62869767  62869769  62953079  62993667  62993703  63034232  63038804  63044938  63068954  63068955  63068957  63076577  63081279  63094534  63094538  63102051  63128592  63128593  62521418R  62939011R  63128592R  77002646R",
      "center_classification_date": "20180705",
      "distribution_pattern": "Products were distributed solely to Japan.",
      "state": "IN",
      "product_description": "Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 13.5; 00-7713-013-00",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2368-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80188",
      "termination_date": "20200528",
      "more_code_info": "",
      "recall_initiation_date": "20180530",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}