{
  "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": "Palm Beach Gardens",
      "address_1": "4500 Riverside Drive",
      "reason_for_recall": "Anspach Effort, Inc.  Palm Beach Gardens, FL is recalling their Single Use Sterile Bone Cutting Burrs used with XMax, microMax, microMax Plus, eMax, eMax2 and eMax2 Plus High Speed Drill Systems.  It is possible for the cutter to come apart.",
      "address_2": "",
      "product_quantity": "5 each",
      "code_info": "Lot numbers E203050779 and E383055709.",
      "center_classification_date": "20120725",
      "distribution_pattern": "US Nationwide Distribution including the states of: Arizona. and California.",
      "state": "FL",
      "product_description": ".***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop.  Use with SHORT-HD Attachment ***RX Only      Product Usage:  Cutting and shaping bone including bones of the spine and cranium.",
      "report_date": "20120801",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "The Anspach Effort, Inc.",
      "recall_number": "Z-2077-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62326",
      "termination_date": "20130725",
      "more_code_info": "",
      "recall_initiation_date": "20110919",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}