{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hilden",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92609",
      "recalling_firm": "Qiagen GmbH",
      "address_1": "Qiagen Str. 1",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "DC, AL, CA, FL, GA, ME, NC, NY, OR, TX Foreign:  DE, AE, AT, BE, BG, CH, CL, CY, CZ, DE, DK, ES, FI, FR, GB, GR, GT, HK, HU, ID, IN, IT, JO, MC, MU, MY, NL, NA, PL, PT, RO, SE, SK, TH, TN, TW, UY, YT, ZA",
      "recall_number": "Z-2245-2023",
      "product_description": "QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended for analyzing nasopharyngeal swab (NPS) samples from patients suspected of respiratory infection for the presence of viral or bacterial nucleic acids  REF 691223",
      "product_quantity": "386 kits",
      "reason_for_recall": "Identified a decreased performance reliability rate,  Run abortions could cause delayed diagnosis since sample testing would have to be repeated",
      "recall_initiation_date": "20230519",
      "center_classification_date": "20230727",
      "report_date": "20230802",
      "code_info": "GTIN 14053228038846 LOT Numbers: 175010704, 175011354 Exp.  Date: 2023-10-06 and 2023-10-17"
    }
  ]
}