{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "49146",
      "product_res_number": "Z-0168-2007",
      "event_date_initiated": "2006-10-01",
      "event_date_posted": "2006-11-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-05-13",
      "res_event_number": "36673",
      "product_code": "MMZ",
      "k_numbers": [
        "K033335"
      ],
      "product_description": "Modularis URO urological table Model number 5531012",
      "code_info": "Model number 5531012, serial numbers 01001 to 01345",
      "firm_fei_number": "2240869",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "city": "Malvern",
      "state": "PA",
      "postal_code": "19355-1406",
      "additional_info_contact": "Roland Richter\n610-448-4500",
      "reason_for_recall": "Potential pinch point with the patient table",
      "root_cause_description": "Other",
      "action": "The recalling firm has issued a Customer Safety Advisory to affected customers per Update Instructions SPO23/06/S. This letter, to be inserted in the system Operator Manual, reminds customers of the potential pinch point and provides a suggestion to avoid its occurrence.",
      "product_quantity": "59 units",
      "distribution_pattern": "Nationwide.",
      "openfda": {
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        "k_number": [
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        "device_name": "Table, Cystometric, Electric",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4890",
        "device_class": "2"
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}