{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "4141 Directors Row",
      "reason_for_recall": "Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger Release Blades which could not be advanced into the cannula through which it is used during trigger finger release procedures.",
      "address_2": "Ste. H",
      "product_quantity": "235",
      "code_info": "Model number 1052; Lots M674180, MAKL170, M674200",
      "center_classification_date": "20130308",
      "distribution_pattern": "USA Nationwide Distribution including the states of: AZ, MI, NE, NV, and TX.",
      "state": "TX",
      "product_description": "Endotrig Trigger Release Sterile Micro Hook Blade    Product Usage:  The blade is intended to release A-1 pulley in endoscopic trigger release procedures.",
      "report_date": "20130320",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Instratek, Incorporated",
      "recall_number": "Z-0922-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63551",
      "termination_date": "20130410",
      "more_code_info": "",
      "recall_initiation_date": "20120918",
      "postal_code": "77092-8743",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}