{
  "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": [
    {
      "status": "Terminated",
      "city": "North Brunswick",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71973",
      "recalling_firm": "Ohm Laboratories, Inc.",
      "address_1": "1385 Livingston Ave",
      "address_2": "N/A",
      "postal_code": "08902-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-0037-2016",
      "product_description": "Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 49348-930-01, UPC 0 1093936544 6); and b)  30-count tablets per box (NDC 49348-930-44, UPC 0 1093934944 6) Distributed by McKesson, One Post Street, San Francisco, CA  94104",
      "product_quantity": "N/A",
      "reason_for_recall": "Superpotent Drug: Out Of Specification (OOS) result for Assay.",
      "recall_initiation_date": "20150728",
      "center_classification_date": "20151015",
      "termination_date": "20161028",
      "report_date": "20151021",
      "code_info": "Batch Numbers:    (a) 2544488, Exp 7/31/2016; 26917891, Exp 5/31/2016.  (b) 2544488, Exp 7/31/2016; 2617893, Exp 5/31/2016; 2644273, Exp 9/30/2016"
    }
  ]
}