{
  "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": "Bedford",
      "address_1": "300 Northfield Rd",
      "reason_for_recall": "Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.",
      "address_2": "",
      "product_quantity": "6,515 packs",
      "code_info": "Lot # 2006500, Exp 08/31/12",
      "center_classification_date": "20120614",
      "distribution_pattern": "Nationwide and Puerto Rico.",
      "state": "OH",
      "product_description": "Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials per pack, Rx only, Manufactured for: Bedford Laboratories, Bedford, OH  44146; Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH  44146; NDC 55390-160-10; UPC 3 55390-160-10 1.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ben Venue Laboratories Inc",
      "recall_number": "D-1377-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "61802",
      "termination_date": "20130821",
      "more_code_info": "",
      "recall_initiation_date": "20120501",
      "postal_code": "44146",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}