Device recall

Z-0163-2007: 1.5T HD Head Neck Spine Array, Model 2416329, for GE 1.5T Excite MR System.

FDA device recall · Class II · USA Instruments Incorporated

Key facts

Recall number (Z-number) Z-0163-2007
Recall event 36612
Product 1.5T HD Head Neck Spine Array, Model 2416329, for GE 1.5T Excite MR System.
Product code MOS
Recalling firm USA Instruments Incorporated
Recall class Class II
Status Terminated
Termination date Apr 13, 2012
510(k) numbers K052621
FEI number 3005214683

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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

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