{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 19
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  },
  "results": [
    {
      "cfres_id": "91041",
      "product_res_number": "Z-1684-2010",
      "event_date_initiated": "2010-04-20",
      "event_date_posted": "2010-05-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-01-06",
      "res_event_number": "55529",
      "product_code": "MDR",
      "product_description": "Juxta-Lite compression wrap Large Short 28cm Length with Anklet Catalog 23025017",
      "code_info": "All units sold between 2/1/10 and 4/14/10.",
      "firm_fei_number": "2243150",
      "recalling_firm": "Circaid Medical Products Inc",
      "address_1": "9323 Chesapeake Dr Ste B1/B2",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92123",
      "additional_info_contact": "858-576-3550",
      "reason_for_recall": "Some systems in these lots have Built-In Pressure System lines with the incorrect amount of spacing. Some systems in these lots had I inch space between each line with no tension applied. The system should have 1.25 inches of space. The correct spacing (1.25\") is necessary to achieve the measured tension ranges. The incorrect spacing may result in the inability to achieve the correct tension level",
      "root_cause_description": "Process control",
      "action": "CircAid Medical Products Important Device Product Recall  letter dated Apr 20, 2010 was mailed to consignees describing problem, listing affected product and distribution dates.  Customers were instructed to locate and return these Juxta-Lite Systems from stock and notify their customers  A Retum Authorization number and contact name was provided.\nthis listing for product returns.",
      "product_quantity": "372 total, all sizes",
      "distribution_pattern": "Worldwide distribution: USA, Japan, Canada, Netherlands",
      "openfda": {
        "registration_number": [
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        "device_name": "Binder, Medical, Therapeutic",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5160",
        "device_class": "1"
      }
    }
  ]
}