{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Allentown",
      "address_1": "901 Marcon Blvd",
      "reason_for_recall": "B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI convenience kits containing the 22GA 1-1/2in SafetyGlide Needle due to the presence of loose polypropylene foreign matter was above release specification. This foreign matter has been  identified as a product hub material which has been tested for biocompatibility per ISO 10993 during the product  development process.",
      "address_2": "",
      "product_quantity": "700 units",
      "code_info": "0061525340.  0061535836.",
      "center_classification_date": "20180209",
      "distribution_pattern": "US Nationwide Distribution.",
      "state": "PA",
      "product_description": "PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590.     Local anesthesia of the skin prior to insertion of the regional anesthesia needle.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "B. Braun Medical, Inc.",
      "recall_number": "Z-0572-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78878",
      "termination_date": "20180403",
      "more_code_info": "",
      "recall_initiation_date": "20170621",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}