{
  "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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      "city": "Cambridge",
      "state": "MA",
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      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Philips North America",
      "address_1": "222 Jacobs St",
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      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-0975-2024",
      "product_description": "Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system",
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      "reason_for_recall": "Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.",
      "recall_initiation_date": "20220106",
      "center_classification_date": "20240202",
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