{
  "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": "2026-04-22",
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    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.",
      "address_2": "",
      "product_quantity": "64 units",
      "code_info": "Serial Numbers:  0000000010-203  0000000010-191  000003100-1829  00008125-18-18  00000000010-15  00000000010-63  00008125-16-59  000000099-4-04  00000000010-31  00000000010-82  00008125-16-70  00008125-18-09  00008125-18-16  00000000017-64  10280  00000000010-30  000003681-1803  00000000018-24  000003100-1840  000003101-1502  000003100-1744  00000000017-36  00000000016-86  00000000017-31  1065  1998  1999  000008125-1630  1008  00000000017-20  00000000017-22  00000000017-23  1804  00000000030-14  00000000030-15  00000000010-37  00000000010-44  00000000010-55  00000000030-16  00000000018-39  1704  00000ICPO50612  1697  1696  000000163-1758  00000000018-23  00000000016-73  00000000030-04  00000000010-59  00000000018-22  000003100-1760  000003100-1743  0000000010-134  000003100-1719  343  000003100-1763  61061  00000000010-04  00000000030-11  1649  00000000010-67  00000000010-45  00000000017-27  00000000017-15",
      "center_classification_date": "20190109",
      "distribution_pattern": "Worldwide",
      "state": "WI",
      "product_description": "VariCam",
      "report_date": "20190116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-0704-2019",
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      "event_id": "81736",
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      "recall_initiation_date": "20171030",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
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}