{
  "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": {
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    {
      "country": "United States",
      "city": "Cranbury",
      "address_1": "270 Prospect Plains Rd",
      "reason_for_recall": "Failed Impurities/Degradation Specifications",
      "address_2": "",
      "product_quantity": "4,656 HDPE bottles",
      "code_info": "Lot #: AVF0246/A,  AVF0247/B,  AVF0246/B,  AVF0246/C; Exp. 02/17",
      "center_classification_date": "20160916",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count bottle (NDC 57664-242-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u.  29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512",
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      "recall_initiation_date": "20160627",
      "postal_code": "08512-3605",
      "voluntary_mandated": "Voluntary: Firm initiated",
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