{
  "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": "Ongoing",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89753",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "1 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in the US and territories, Japan, and Canada",
      "recall_number": "Z-0915-2022",
      "product_description": "ROTAWIRE Drive and wireClip Torquer, ROTAWIRE Drive Floppy",
      "product_quantity": "433 5-packs",
      "reason_for_recall": "Pouch seals may be open, compromising sterility.",
      "recall_initiation_date": "20220308",
      "center_classification_date": "20220412",
      "report_date": "20220420",
      "code_info": "ROTAWIRE Drive Floppy, 5 pack, UPN: H74939462005  Individual units within 5-pack are labeled as Single, UPN: H74939462001  Batch numbers: 27622475, 27622478, 27691111, 27698472, 27706785, 27708190, 27756019 27756205, 27756933, and 27756935  GTIN: 08714729996255"
    }
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}