{
  "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": [
    {
      "status": "Terminated",
      "city": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86608",
      "recalling_firm": "Micro-Tech Usa",
      "address_1": "2855 Boardwalk St",
      "address_2": "N/A",
      "postal_code": "48104-6715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of AZ, CA, CO, CT, IL, MA, MI, NY, OH, PR, TX, VA. No OUS distribution.",
      "recall_number": "Z-0470-2021",
      "product_description": "Elastic Traction Device, 11mm Lower. UPN: ER56041  Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use in flexible Endoscopy to provide retraction to assist in tissue resection, exposure, and removal of tissue within the gastrointestinal tract.",
      "product_quantity": "2420 pieces",
      "reason_for_recall": "FDA has informed Micro-Tech that the Elastic Traction Device is not appropriately classified as a Class I device and requires 510(k) clearance to be marketed in the US.",
      "recall_initiation_date": "20201005",
      "center_classification_date": "20201118",
      "termination_date": "20211202",
      "report_date": "20201125",
      "code_info": "Lots M190808231  M191018231  M191224231  M200305232"
    }
  ]
}