{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wall Township",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83285",
      "recalling_firm": "Alto Development Corp",
      "address_1": "5206 Asbury Rd",
      "address_2": "N/A",
      "postal_code": "07727-3609",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution US Nationwide, Czech Republic, Italy, Israel, and UK.",
      "recall_number": "Z-2098-2019",
      "product_description": "A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire Looped Electrode (M-21 SERIES)-  Temporary Pacing Electrode as follows:  021-001 MYO/Wire Ultra-Flex Monopolar (Wht.,2-0)  021-010 MYO/Wire Ultra-Flex Monopolar (Org.,2-0)  021-011 MYO/Wire Ultra-Flex Monopolar (Wht.,2-0)    Used as a connection between temporary cardiac pacing or monitoring equipment and the heart.",
      "product_quantity": "351.5 Boxes",
      "reason_for_recall": "Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire looped electrode (M-21 Series)  to be consistent between electrode IFU and instructions for M-21 loop.",
      "recall_initiation_date": "20190621",
      "center_classification_date": "20190729",
      "termination_date": "20200513",
      "report_date": "20190807",
      "code_info": "Lots 0715A or later"
    }
  ]
}