{
  "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": "Plymouth",
      "address_1": "44650 Helm Ct",
      "reason_for_recall": "Shipped femur guide contained a non-conformance which could possibly impact fit of the drill insert.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Lot 094929",
      "center_classification_date": "20140103",
      "distribution_pattern": "US Distribution: MO only.",
      "state": "MI",
      "product_description": "REF 42-411571  QTY 1 CATALOG  CAUTION. SEE INSTRUCTIONS FOR USE  SIGNATURE  M PKA GDE/MDL SET SML-MP  DD.....R-FEB55RKA-T JA-A01 05551  PKA POST CUT SML-PKA MICROPLASTY  CUSTOM-MADE DEVICE  non-sterile    The Signature Personalized Patient Care System includes the patient-specific Signature Guides which are patient specific instruments (guides are considered custom-made per EU definition) intended for use during the surgical procedure for total and partial knee arthroplasty.",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Materialise USA LLC",
      "recall_number": "Z-0628-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "67039",
      "termination_date": "20140114",
      "more_code_info": "",
      "recall_initiation_date": "20131126",
      "postal_code": "48170-6061",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}