{
  "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": {
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      "product_res_number": "Z-0574-04",
      "event_date_initiated": "2004-01-26",
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      "recall_status": "Terminated",
      "event_date_terminated": "2015-06-11",
      "res_event_number": "28223",
      "product_code": "FPB",
      "product_description": "Millex-HA Syringe Driven Filter Unit, 0.45 um, Sterile\nCatalog Number: SLHAM33SS",
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      "recalling_firm": "Millipore Corp.",
      "address_1": "80 Ashby Rd",
      "city": "Bedford",
      "state": "MA",
      "postal_code": "01730-2237",
      "additional_info_contact": "Thomas Borrows\n781-533-2622",
      "reason_for_recall": "Lack of assurance of sterility",
      "root_cause_description": "Other",
      "action": "Millipore notified direct and distributor accounts by Certified letter on 1/26/04. Users are requested to return product. Millipore France and Ireland coordinating recall to the international accounts.",
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        "medical_specialty_description": "General Hospital",
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