Device recall

Z-0507-2012: Microsoft Amalga Unified Intelligence System (UIS), This is a software-only…

FDA device recall · Class II · Microsoft Corporation Health Solutions Group

Key facts

Recall number (Z-number) Z-0507-2012
Recall event 56545
Product Microsoft Amalga Unified Intelligence System (UIS), This is a software-only device, WHIE Implementation v1.1i. A calculator/data processing module, for clinical use. Intended to provide the clinical user with the ability to view data from multiple, different data systems.
Product code JQP
Recalling firm Microsoft Corporation Health Solutions Group
Recall class Class II
Status Terminated
Termination date Dec 20, 2011
FEI number 3007734659

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)