{
  "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": "665",
      "code_info": "60936172  61002401  61150834  61326535  61332941  61359861  61375746  61403159  61409715  61459935  61479150  61559581  61729731  61741696  61757673  62014555  62014556  62014557  62059105  62071437  62118877  62130043  62163680  62207789  62282107  62323345  62356227  62420836  62432974  62503175  62521427  62560139  62578410  62586781  62616563  62647184  62659327  62694084  62707654  62721037  62782080  62803651  62927127  62939025  62953083  63063349  63063351  63063352  63068972  63090045  63090046  63090047  63116808  63116809  63116810  77004216  61590535R  62071437R",
      "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 16.25; 00-7713-016-00",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2370-2018",
      "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"
    }
  ]
}