{
  "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": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Zimmer Biomet is conducting a voluntary recall for a single lot of the Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System after it was determined that two pieces from the lot were moved to finished goods and shipped despite having an open Non-Conformance Report (NCR). The NCR indicated that one piece from the lot had scratches and the other non-confirming threads.",
      "address_2": "",
      "product_quantity": "16",
      "code_info": "Model Number: 113956, Modular Hybrid Glenoid Base Large, Item Number: 113956,  Lot Number: 270260,  UDI Number: (01) 00880304462618 (17) 211204 (10) 270260",
      "center_classification_date": "20170601",
      "distribution_pattern": "Worldwide Distribution - US including OH AZ ID PA AR MN IL CA MD CA MN NY  Foreign: Canada",
      "state": "IN",
      "product_description": "Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with an Argon flush. The vacuum sealed product is then placed into a Tyvek/film pouch and that pouch is heat sealed. The fully pouched product is then labeled and placed into a carton with an IFU. The carton is then labeled and shrink wrapped. The labels also include a sterilization indication dot.  This system is intended for primary and revision total shoulder arthroplasty, as well as hemi-arthroplasty",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2216-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77119",
      "termination_date": "20180330",
      "more_code_info": "",
      "recall_initiation_date": "20170426",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}