{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "There is a potential for silicone shedding during cleaning and sterilization.",
      "address_2": "",
      "product_quantity": "971 in total",
      "code_info": "Lot Numbers 453392  453918  453919  469917  475577  481064  481065  486820  498695  506818  512867  512868",
      "center_classification_date": "20190114",
      "distribution_pattern": "Worldwide Distribution - US Nationwide,  The products were distributed to the following foreign countries:  Australia, Chile, Netherlands.",
      "state": "IN",
      "product_description": "Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003    Product Usage:  Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals",
      "report_date": "20190123",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0735-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81758",
      "termination_date": "20200512",
      "more_code_info": "",
      "recall_initiation_date": "20181128",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}