{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Marcy L'Etoile",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87985",
      "recalling_firm": "BioMerieux SA",
      "address_1": "Chemin De L'Orme",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in the U.S. was nationwide.  There was also military and government distribution.",
      "recall_number": "Z-2225-2021",
      "product_description": "MYLA software.  Used to manage microbiology test workflow from the reception of requests to the transmission of results by transferring, storing, and displaying medical device data.",
      "product_quantity": "248 systems",
      "reason_for_recall": "Software anomaly - Under certain conditions, unwanted alterations to results could be applied when using the BCI Connect scripting feature.",
      "recall_initiation_date": "20210622",
      "center_classification_date": "20210806",
      "termination_date": "20230206",
      "report_date": "20210818",
      "code_info": "MYLA V4.8.0/4.8.1 and MYLA V4.7.0/V4.7.1 in conjunction with BCI CONNECT, UDI 03573026619244 and 03573026610975."
    }
  ]
}