{
  "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": "Plymouth",
      "address_1": "2905 Northwest Blvd Ste 40",
      "reason_for_recall": "Mislabeled.  Packages labeled PFSI-00053, Right Lateral/Left Medial contains PFSI-00054, Right Medial/Left lateral implants.  Packages labeled PFSI-00054, Stride Right Medial/Left Lateral contain PFSI-00053, Left Medial/Right Lateral.",
      "address_2": "",
      "product_quantity": "2",
      "code_info": "Lot C785241, Exp 4-2015",
      "center_classification_date": "20140627",
      "distribution_pattern": "US Nationwide Distribution in the states of CA, PA, and TX",
      "state": "MN",
      "product_description": "Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Blue Belt Technologies MN",
      "recall_number": "Z-1943-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68482",
      "termination_date": "20140804",
      "more_code_info": "",
      "recall_initiation_date": "20140604",
      "postal_code": "55441-2673",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}