{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "BD Diagnostic Systems",
      "reason_for_recall": "A low level of surface and subsurface contamination of Listeria monocytogenes on 9 lots of non-sterile prepared plated media containing sheep blood, typically visible immediately upon removal from the packaging. The contamination is typically observed as 1-3 CFUs per plate when present.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "775 cases",
      "code_info": "Catalogue # 221263 with Lot #4099228",
      "center_classification_date": "20150114",
      "distribution_pattern": "Worldwide Distribution - US nationwide including Puerto Rico, Belgium, Canada, Philippines, Singapore, and Taiwan.",
      "state": "MD",
      "product_description": "Columbia Agar with 5% Sheep Blood    Columbia Agar with 5% Sheep Blood is a general purpose culture medium used for the growth and recovery of fastidious microbial species.",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-0976-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69091",
      "termination_date": "20160812",
      "more_code_info": "",
      "recall_initiation_date": "20140606",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}