{
  "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": "Minnetonka",
      "address_1": "5929 Baker Rd Ste 470",
      "reason_for_recall": "This recall has been initiated because the Arobella Medical 6mm Qurette Q07 Lot Numbers 0001 and 0002 can fracture during use and may release a fragment or fragments. The 6 mm Qurette is a component of the AR1000 Quostic Wound Therapy System.",
      "address_2": "",
      "product_quantity": "99",
      "code_info": "0001 and  0002",
      "center_classification_date": "20121217",
      "distribution_pattern": "Worldwide distribution - US (nationwide) and the states of AL, CA, ID, IN, IA, MI, MN, MS, NJ, NM, OH, PA. SC, TX, UT, VA, WI. including the country of SAUDI ARABIA.",
      "state": "MN",
      "product_description": "Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Wound Therapy System.     Major components of the AR1000 Wound Therapy System include an ultrasonic generator, converter hand piece, done-shaped applicator tip (qurette), and a saline supply reservoir.     Product Usage:  The Arobella Medical AR1000 Wound Therapy System is interned for the selective dissection and fragmentation of tissue, wound debridement ( of acute and chronic wounds, burns, and diseased or necrotic tissue), and cleansing irrigation of the wound site for the removal of debris, exudates, fragments, and other matter.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arobella Medical, LLC",
      "recall_number": "Z-0534-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63808",
      "termination_date": "20150304",
      "more_code_info": "",
      "recall_initiation_date": "20121105",
      "postal_code": "55345-4770",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}