{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "29459",
      "product_res_number": "Z-0029-04",
      "event_date_initiated": "2003-09-05",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-11",
      "res_event_number": "27225",
      "product_description": "Dow Corning Silastic brand Medical Adhesive Silicone, Type A, non-sterile, 57 gram tube; material numbers 3242901 (100 tubes) and 3242897 (6 tubes).",
      "code_info": "material number 3242901; lots 0001531727, 001583486 and 0001671243.  material number 3242897; lot 0001604743.",
      "firm_fei_number": "1824893",
      "recalling_firm": "Dow Corning Corp.",
      "address_1": "12334 Geddes Rd.",
      "city": "Hemlock",
      "state": "MI",
      "postal_code": "48626",
      "additional_info_contact": "989-496-1680",
      "reason_for_recall": "May be contaminated with iron, chromium and nickel from stainless steel equipment failure during manufacture.",
      "root_cause_description": "Other",
      "action": "Customers were notified via phone call and by letter dated September 5, 2003.  Customer were asked to return unused materials.",
      "product_quantity": "2300",
      "distribution_pattern": "United States.",
      "openfda": {}
    }
  ]
}