{
  "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": [
    {
      "country": "United States",
      "city": "Pine Brook",
      "address_1": "26 Chapin Rd",
      "reason_for_recall": "Presence of Foreign Matter: Guaifenesin API powder is being recalled due to the possibility that the product contains polyethylene fibers from a screen used to sift the Guaifenesin.",
      "address_2": "Suite 1103",
      "product_quantity": "30,800 Kg",
      "code_info": "211J3291  211J3292  211K3293  211K3294  211K3295  211K3297  211K3298  211K3299  211K3301  211K3302  211K3315  211K3321  211K3322",
      "center_classification_date": "20140318",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Guaifenesin USP, 50 Kg Drums, CAS No. 93-14-1, Reg. No. 05436, Caution: For Manufacturing, Processing, or Repacking, Delta Synthetic Co., Ltd. 15, Minsheng St., Tucheng Dist., New Taipei City, 23679, Taiwan (ROC), NDC 60203-1001",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Traxx International Corp",
      "recall_number": "D-1165-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "67661",
      "termination_date": "20170926",
      "more_code_info": "",
      "recall_initiation_date": "20140114",
      "postal_code": "07058-9210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}