{
  "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": "Portland",
      "state": "OR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87036",
      "recalling_firm": "Riverpoint Medical, LLC",
      "address_1": "825 NE 25th Ave",
      "address_2": "",
      "postal_code": "97232-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: NJ  OUS: Germany, Croatia, Italy, India, Poland and Spain.",
      "recall_number": "Z-0949-2021",
      "product_description": "Covidien CV-9590 Velosorb Fast Braided Fast absorbable Suture 14 Metric 36\" 90 cm, GS-24 Taper 1/2 40 mm, undyed, UDI: 10884521151307",
      "product_quantity": "3060 units",
      "reason_for_recall": "Due to a manufacturing error, there is a potential that sutures may exhibit inadequate tensile strength.  This could potentially lead to intra-operative and post-operative complications such as suture break or wound dehiscence.",
      "recall_initiation_date": "20201209",
      "center_classification_date": "20210203",
      "termination_date": "20230421",
      "report_date": "20210210",
      "code_info": "Lot # 19062715X",
      "more_code_info": ""
    }
  ]
}