{
  "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": "Columbus",
      "address_1": "2550 John Glenn Ave",
      "reason_for_recall": "Failed USP Dissolution Test Requirements: This sub-recall is in response to Prometheus Laboratories Inc. recall for Mercaptopurine USP 50mg because the lot does not meet the specification for dissolution.",
      "address_2": "Suite A",
      "product_quantity": "3496 cartons",
      "code_info": "Lot #: 142450 Exp 05/2015; 140862 Exp 02/2015; 141596 Exp 03/2015; 134770 Exp 01/2015",
      "center_classification_date": "20141216",
      "distribution_pattern": "Nationwide.",
      "state": "OH",
      "product_description": "Mercaptopurine Tablets, USP, 50 mg, 30 Tablets (3 x 10) unit dose blisters per carton, Rx only, Manufactured by Prometheus Laboratories Inc. 9410 Carroll Park Drive, San Diego, CA 92121, repackaged by American Health Packaging 2550-A John Glenn Avenue, Columbus, OH 43217, NDC 68084-325-21",
      "report_date": "20141224",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "American Health Packaging",
      "recall_number": "D-0300-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "69972",
      "termination_date": "20150601",
      "recall_initiation_date": "20141119",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}