{
  "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": "Terminated",
      "city": "Breinigsville",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89660",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "200 Boulder Dr",
      "address_2": "N/A",
      "postal_code": "18031-1532",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: MA, VT",
      "recall_number": "Z-0819-2022",
      "product_description": "PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions  Catalog Number: 8713030U",
      "product_quantity": "6 units",
      "reason_for_recall": "Units not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in delays in  therapy, overinfusion, or underinfusion.",
      "recall_initiation_date": "20220207",
      "center_classification_date": "20220322",
      "termination_date": "20231228",
      "report_date": "20220330",
      "code_info": "Serial Numbers: 633299, 633307, 633310, 633313, 633315, 633318 GUIDID: 04046963716745"
    }
  ]
}