{
  "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": "Palm Beach Gardens",
      "address_1": "4500 Riverside Dr",
      "reason_for_recall": "The potential exists for the Oscillating Saw Attachment to disengage from the Small Battery Drive handpiece.  If the attachment disengages from the handpiece intra-operatively, there is a potential for injury to the patient and/or user.",
      "address_2": "",
      "product_quantity": "12,085 pieces",
      "code_info": "ALL Lots",
      "center_classification_date": "20150430",
      "distribution_pattern": "Worldwide Distribution - US (nationwide including DC, Hawaii, and Puerto Rico) and Internationally to Argentina, Austria, Australia, Belgium, Bahrain, Bolivia, Brazil, Canada, China, Chile, Costa Rica, Czech Republic, Germany, Denmark, Ecuador, Egypt, Spain, Finland, France, Great Britain, Greece, Guatemala, Hong Kong, Croatia, Hungary, Indonesia, Ireland, Israel, India, Iraq, Iran, Italy, Jordan, Japan, Kenya, Korea, Kuwait, Lebanon, Sri Lanka, Libyan Arab Jamahiriya, Morocco, Macedonia, Mexico, Malaysia, Netherlands, Norway, Nepal, New Zealand, Oman, Ontario, Peru, Philippines, Palestine, Portugal, Romania, Serbia, Russian Federation, Saudi Arabia, Sweden, Singapore, Slovenia, Slovakia, South Africa, El Salvador, Thailand, Turkey, Taiwan, Ukraine, Uruguay, Venezuela, Vietnam and United Arab Emirates.",
      "state": "FL",
      "product_description": "Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021  for orthopedic surgery.",
      "report_date": "20150506",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "The Anspach Effort, Inc.",
      "recall_number": "Z-1553-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70919",
      "termination_date": "20161214",
      "more_code_info": "",
      "recall_initiation_date": "20150324",
      "postal_code": "33410-4235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}