{
  "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": [
    {
      "status": "Terminated",
      "city": "Charlottesville",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73373",
      "recalling_firm": "MicroAire Surgical Instruments, LLC",
      "address_1": "3590 Grand Forks Blvd",
      "address_2": "N/A",
      "postal_code": "22911-9006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "recall_number": "Z-1328-2016",
      "product_description": "MicroAire PAL¿ Cannula     Product Usage - Power Aspiration Device",
      "product_quantity": "145 manufactured and distributed",
      "reason_for_recall": "MicroAire has initiated a recall on product  PAL-R4011XL (40cm x 4mm Del Vecchio French Rasp cannula), due to our receipt of three (3) complaints that it bent or broke during surgery.    Accordingly, the PAL-R4011XL has also been put on production hold until further notice.",
      "recall_initiation_date": "20160208",
      "center_classification_date": "20160405",
      "termination_date": "20170214",
      "report_date": "20160413",
      "code_info": "Include lot numbers/serial numbers    0913228216, 0414243005, 0215266350, 0415269875, 0515271334",
      "more_code_info": ""
    }
  ]
}