Device Recall DEXIS Imaging Suite 의 리콜

Recall

62830

Class 2

Z-2463-2012

2012-07-30

2012-09-26

Terminated

United States

2016-10-13

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=111796

A condition can occur during renumbering of the patient database using the dexcopy feature. when renumbering is being performed using the dexcopy feature and multiple patients with an identical name are present, the software will assign all subsequent records to the first patient record, resulting in mixed patient records. in order for this problem to occur several conditions need to be met: 1).

DEXIS sent a Medical Device Corrective Action letter dated July 30, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. An Acknowledgement Form was included with the notification that is to be returned by the consignee to the recalling firm. Customers were instructed to call DEXIS Technical Support at 888-883-3947 as soon as possible to have Technical Support review and potentially correct any issues that may have resulted from its use. To request a free-of-charge upgrade kit, customers should email a request to orders@dexis.com. For questions regarding this recall call 215-997-5666,