Events

Retiro De Equipo (Recall) de Device Recall Aperio ScanScope System

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Aperio Technologies Inc.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    33728
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1549-2013
  • Fecha de inicio del evento
    2013-02-22
  • Fecha de publicación del evento
    2013-06-17
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2013-09-25
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=42354
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Microscope, phase contrast - Product Code IBM
  • Causa
    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.
  • Acción
    Aperio sent an Urgent Medical Device Recall letter dated April 22, 2013 to all affected consignees via certified USPS mail. The letter included the reason for the recall, recall product information, instructions, acknowledgement form, contact information ( Aperio Technical Support at 1-866-478-3999), and product labeling. The consignees were requested to acknowledge receipt of the Medical Device Correction letter. In addition, an Acknowledgement Form is required to be signed and e-mailed back to the Manufacturer as evidence of letter receipt. For questions regarding this recall call 760-304-6211, ext 6211.

Device

Device Recall Aperio ScanScope System
  • Modelo / Serial
    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
  • Clasificación del producto
    Hematology and Pathology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution - including all states, none internationally .
  • Descripción del producto
    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.
  • Manufacturer
    Aperio Technologies Inc

Manufacturer

Aperio Technologies Inc
  • Dirección del fabricante
    Aperio Technologies Inc, 1360 Park Center DR, Vista CA 92081-8300
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Source
    USFDA