{
  "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": "2026-08-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99300",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "100 Boston Scientific Way",
      "address_2": "",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN,  KY, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NM, NY, OH, PA, PR, SC, TN, TX, UT, VA, VT, WA, WI and International distribution pending.",
      "recall_number": "Z-2840-2026",
      "product_description": "Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN:      Radial Jaw 4 Jumbo 240cm   Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.",
      "product_quantity": "5,020 (US); 20,770 (OUS)",
      "reason_for_recall": "Potential for breach in sterile barrier of device packaging.",
      "recall_initiation_date": "20260630",
      "center_classification_date": "20260731",
      "report_date": "20260812",
      "code_info": "Outer Box UPN: M00513363; Inner Box UPN: M00513360. GTIN: 08714729761914. Lot Number: 38496094.",
      "more_code_info": ""
    }
  ]
}