Skip to content
Recall Observatory FDA recall evidence

Device product

MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.

Z-1365-2013

May 07, 2013

Class II

Product summary

Firm
Medical Information Technology, Inc.
Event
Event 65158
Status
Terminated
Classification
Class II
Quantity
56 devices
Official record key
device-enforcement:Z-1365-2013

Official wording

Reason: Incorrect transmission of laboratory results.

Code information: Magic Releases 5.41, 5.52. 5.53, 5.62, 5.63, 5.64 and Client Server Releases 5.64, 5.65, 6.05, 6.06, 6.07

Distribution pattern: Worldwide Distribution - USA, including Puerto Rico and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Incorrect transmission of laboratory results.