{
  "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": "Terminated",
      "city": "Concord",
      "state": "NC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63127",
      "recalling_firm": "McKesson Packaging Services",
      "address_1": "7101 Weddington Rd NW",
      "address_2": "N/A",
      "postal_code": "28027-3412",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-001-2013",
      "product_description": "buPROPion Hydrochloride Extended-Release Tablets (XL), 150 mg, UD 100 Tablets (10 x 10) per carton, Rx only, Mfg By: CMIC-VPS Corporation, Cranbury, New Jersey  08512; blister barcode N (01)003 63739 449 10 7, Dist By: McKesson Packaging, Concord, NC  28027; NDC 63739-449-10, carton barcode 6373944910.",
      "product_quantity": "187 cartons",
      "reason_for_recall": "Failed USP Dissolution Test Requirements: Possible out-of-specification dissolution results at the 8 hour stability testing point.",
      "recall_initiation_date": "20120329",
      "center_classification_date": "20121001",
      "termination_date": "20130411",
      "report_date": "20121010",
      "code_info": "Lot #: 0074583, Exp. Date 03/12"
    }
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}