{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Vista",
      "address_1": "1360 Park Center DR",
      "reason_for_recall": "Aperio initiated this recall because the User Guides incorrectly state the devices had been cleared for specific applications. The User Guides should state the devices are for Research Use Only and are not for use in diagnostic procedures.",
      "address_2": "",
      "product_quantity": "364",
      "code_info": "The following serial numbers of the Aperio ScanScope systems are affected in the USA by this recall:    ¿ScanScope XT  ScanScope AT  ScanScope ATT  ScanScope es, esa     1223, 1273, 1278, 1277, 1282,  1593,1605,  1648,1657,1660,  5064,5068,5108,5155,5170,5171     1285,1286,1287,1293,1296,  1619, 1620,  1662,1663,1666,  5176,5181,5187,5196,5198,5202,     1299,1300,1301,1302,1304,  1623, 1633,  1671, 1672, 1673,  5204,5205,5233,5236,5237,5241,     1311,1312,1314,1315,1316,  1634,1635,  1676, 1678, 1679,  5244,5245,5246,5248,5253,5262,     1318,1319,1320,1321,1322,  1636, 1637,  1690, 1692, 1695,  5266,5267,5269,5270,5272,5276,     1324,1325,1327,1328,1330,  1638,1640,  1698,1700,1718  5277,5279,5283,5287,5288,5293,     1332, 1333, 1335, 1336, 1338,  1643,1645,   5294, 5295, 5302, 5307, 5308, 5309,     1339, 1340, 1342, 1343, 1345,  1649,1654,   5314,5315,5316,5317,5324,5327,     1350,1352,1357,1358,1359,  1656,1664,   5328,5329,5330,5331,5333,5334,     1366, 1368, 1369, 1370, 1372,  1686, 1687,   5336,5339,5340,5341,5345,5347,     1382,1383,1392,1394,1396,  1688, 1689,   5348,5352,5353,5356,5367,5371,     1397, 1399, 1400, 1402, 1404,  1696, 1699,   5374,5379,5381,5388,5390,5394,     1405,1407,1409,1410,1413,  1703,1705,   5396,5402,5403,5404,5405,5406,     1417,1418,1419,1420,1421,  1707, 1708,   5408,5409,5415,5416,5418,5419,     1422, 1423, 1424, 1425, 1426,  1709,1711,   5433,5440,5452,5456,5457,5459,     1436,1441,1442,1444,1445,  1714,1716,   5462,5465,5466,5467,5468,5469,     1446, 1448, 1449, 1450, 1452,  1719,1721,   5470,5473,5475,5476,5477,5478,     1453, 1454, 1456, 1457, 1458,  1723,1724,   5482,5485,5486,5489,5490,5492,     1460,1461,1466,1475,1476,  1725,1727,   5493,5504,5515,5516,5517,5518,     1481,1482,1486,1487,1490,  1728,1729,   5520, 5529, 5537, 5540, 5552, 5566,     1492, 1499, 1500, 1502, 1503,  1731,1733,   5567,5574,5578,5581,5587,5590,     1505,1506,1507,1508,1509,  1735, 1736,   5591,5592,5593     1511,1512,1514,1515,1516,  1739,1744       1517,1519,1520,1522,1523,        1525, 1527, 1528, 1532, 1534,        1535, 1536, 1537, 1538, 1540,        1542,1543,1544,1545,1546,        1547,1548,1549,1550,1551,        1552, 1553, 1554, 1556, 1557,        1559,1560,1563,1564,1569,        1570, 1571, 1575, 1576, 1582,        1586,1587,1588,1590,1591,        1596,1597,1611,1627",
      "center_classification_date": "20130617",
      "distribution_pattern": "Nationwide Distribution - including all states, none internationally    .",
      "state": "CA",
      "product_description": "Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO.  Automated digital slide creation and viewing device.     It is intended to create and view electronic image files representative of tissue specimens fixed to glass slides.",
      "report_date": "20130626",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aperio Technologies Inc",
      "recall_number": "Z-1549-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "33728",
      "termination_date": "20130925",
      "more_code_info": "",
      "recall_initiation_date": "20130222",
      "postal_code": "92081-8300",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}