Device recall

Z-1306-2008: IMPAX 6.2.1 Network Gateway Server, License Key. Catalog # ABC code: EXEGE000…

FDA device recall · Class II · AGFA Corp.

Key facts

Recall number (Z-number) Z-1306-2008
Recall event 46812
Product IMPAX 6.2.1 Network Gateway Server, License Key. Catalog # ABC code: EXEGE000. The product is used to transfer medical imaging data. AGFA Corp., Greenville, South Carolina 2960.
Product code LMD
Recalling firm AGFA Corp.
Recall class Class II
Status Terminated
Termination date Jul 21, 2010
FEI number 3001236302

At a glance

  • None 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

Browse all FDA device recalls (products)