{
  "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": "280",
      "code_info": "61967700  62386066  62386068  62410987  62416627  62445412  62450669  62458974  62472166  62484291  62503192  62515309  62594187  62601210  62615697  62622678  62636747  62665742  62681670  62740032  62797379  62797380  62882393  62917816  62114291R  77003795R",
      "center_classification_date": "20180705",
      "distribution_pattern": "Products were distributed solely to Japan.",
      "state": "IN",
      "product_description": "Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Extended Offset, 00-7711-004-40",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2361-2018",
      "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"
    }
  ]
}