{
  "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": [
    {
      "status": "Terminated",
      "city": "Dover",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71057",
      "recalling_firm": "Zimmer Surgical Inc",
      "address_1": "200 W Ohio Ave",
      "address_2": "N/A",
      "postal_code": "44622-9642",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- US, including the states of AZ, CA, ID, IL, MD, NC, RI, and SC; and, Canada.",
      "recall_number": "Z-1610-2015",
      "product_description": "Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator.  00-2568-000-10.  Zimmer Surgical, Inc.    Intended for post-operative collection of wound drainage.",
      "product_quantity": "36 units",
      "reason_for_recall": "Devices were placed in a shipper carton without the appropriate number of the Instructions for Use (IFU).  Packaging specifications require that each sales unit is accompanied by an IFU. Only one IFU was present in the shipper carton, instead of one IFU per each of the two sales units.",
      "recall_initiation_date": "20150421",
      "center_classification_date": "20150513",
      "termination_date": "20151106",
      "report_date": "20150520",
      "code_info": "Item #00-2568-000-10; Lot #62800843",
      "more_code_info": ""
    }
  ]
}