{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Marysville",
      "address_1": "400 Pyramid Dr",
      "reason_for_recall": "Incorrect dimension on four liners was detected",
      "address_2": "",
      "product_quantity": "12 devices",
      "code_info": "Catalog #: WB-1-1122, Size: 36x52x20, Serial # B13085    Catalog #. WB-1-1110 Size: 36x50x20, Serial # B13099    Catalog # WB-1-1110, Size: 36x50x20, Serial #: B13105    Catalog # WB-1-1110, Size: 36x50x20, Serial # B13106",
      "center_classification_date": "20141021",
      "distribution_pattern": "US Distribution in MO only.",
      "state": "MI",
      "product_description": "Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM F648). Sizes 36x52x20; and 36x50x20.    Device is intended for use with Whiteside Biomechanics, Inc./Signal Medical Corporation Micro-Seal Shell in an uncemented Total Hip Replacement.",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Signal Medical Corporation",
      "recall_number": "Z-0109-2015",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "69418",
      "termination_date": "20150120",
      "more_code_info": "",
      "recall_initiation_date": "20140923",
      "postal_code": "48040-2463",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}