{
  "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": [
    {
      "status": "Completed",
      "city": "Placentia",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87636",
      "recalling_firm": "Bioseal Corporation",
      "address_1": "167 W Orangethorpe Ave",
      "address_2": "N/A",
      "postal_code": "92870-6922",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US: IL and MO  OUS: None",
      "recall_number": "Z-1624-2021",
      "product_description": "Bioseal, Central Line Dressing Kit, containing ChloraPREP Applicator 3 mL, REF: CVC009/20, Sterile EO, Single Use Only,  UDI: (01)00630094430096",
      "product_quantity": "580 units",
      "reason_for_recall": "Pre-op skin prep component ChloraPrep included within kits may allow the growth of Aspergillus penicillioides, which may penetrate the packaging resulting in a breach of the package integrity.",
      "recall_initiation_date": "20210323",
      "center_classification_date": "20210520",
      "report_date": "20210526",
      "code_info": "Affected Lot Numbers: 400521,  400514,  400551,  400556,  400551,  400541,  400536,  400536,  400536  400536,  400536,  400556,  400558"
    }
  ]
}