{
  "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": "Commerce",
      "address_1": "5560 E 61st St",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs",
      "address_2": "",
      "product_quantity": "213,000 capsules",
      "code_info": "1 count blister:  Lot# 01M0412, Exp: 04/15, and Lot#91782, Exp: 01/14.  5 count blister: Lot# 05M0412, Exp: 04/15;   10 count blister:  Lot# 10M0412, Exp: 04/15.",
      "center_classification_date": "20130516",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution Los Angeles, CA 90026.    1 count blister:  UPC 705105524764,  5 count blister: UPC 736211124012,  10 count blister:  UPC 736211123916.",
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      "recalling_firm": "Performance Plus Marketing, Inc.",
      "recall_number": "D-334-2013",
      "initial_firm_notification": "Telephone",
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      "more_code_info": "",
      "recall_initiation_date": "20121217",
      "postal_code": "90040-3406",
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