{
  "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": "Portland",
      "state": "OR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86254",
      "recalling_firm": "Riverpoint Medical, LLC",
      "address_1": "825 NE 25th Ave",
      "address_2": "N/A",
      "postal_code": "97232-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0038-2021",
      "product_description": "Velosorb Fast Braided Absorbable Suture:    Covidien Velosorb 3/0 Undyed 30\" P-11\tSVP2295,\tUDI: 20884521177410 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.",
      "product_quantity": "1260",
      "reason_for_recall": "The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, and increase break strength retention.",
      "recall_initiation_date": "20200803",
      "center_classification_date": "20201001",
      "termination_date": "20220908",
      "report_date": "20201007",
      "code_info": "Lot Number:    20060205FX"
    }
  ]
}