{
  "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": "Houston",
      "address_1": "1304 S Loop W",
      "reason_for_recall": "Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct",
      "address_2": "",
      "product_quantity": "112 bottles",
      "code_info": "Lots: 07272016:03 Expiration Date: 01/23/2017 and 09142016:88 Expiration Date: 03/07/2017",
      "center_classification_date": "20170109",
      "distribution_pattern": "AZ and WA",
      "state": "TX",
      "product_description": "HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20",
      "report_date": "20170118",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Pharm D Solutions, LLC",
      "recall_number": "D-0427-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "75552",
      "termination_date": "20170511",
      "more_code_info": "",
      "recall_initiation_date": "20161012",
      "postal_code": "77054-4010",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}