{
  "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": {
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    {
      "status": "Ongoing",
      "city": "Malvern",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90597",
      "recalling_firm": "MALVERN PANALYTICAL LTD",
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      "address_2": "N/A",
      "postal_code": "N/A",
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      "recall_number": "Z-1442-2022",
      "product_description": "NanoSight NS300",
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      "reason_for_recall": "Product found to not comply to Class 1 Laser safety requirement.",
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      "report_date": "20220810",
      "code_info": "CDRH accession #0510530-003"
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}