{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Montbonnot-Saint-Martin",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96030",
      "recalling_firm": "Tornier S.A.S.",
      "address_1": "161 Rue Lavoisier",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  MN, KY, MD, MA, TX, AK, TX, ID; France, Canada",
      "recall_number": "Z-0846-2025",
      "product_description": "Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200.    Indicated for use during Total Shoulder Arthroplasty.",
      "product_quantity": "24 units",
      "reason_for_recall": "The Pin Guide is being recalled because the metal tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset being unable to detect the Pin Guide and potentially prolonging surgery time or changing of surgical method from guided to conventional.",
      "recall_initiation_date": "20241218",
      "center_classification_date": "20250110",
      "report_date": "20250122",
      "code_info": "UDI/DI 03700434022926, Lot Numbers:  22A796, 22A797, 22A978, and 22A979",
      "more_code_info": ""
    }
  ]
}