{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect which joins the two-halves of the filter cartridge, thus the housing could separate",
      "address_2": "PO Box 610",
      "product_quantity": "1106 boxes (10 filters/box)",
      "code_info": "Lot number: 494604",
      "center_classification_date": "20191017",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "PA",
      "product_description": "Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervical aspiration of the uterine cavity.  Part# 54298-10/pack",
      "report_date": "20191023",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-0159-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83826",
      "recall_initiation_date": "20190912",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}