Device recall

Z-1244-2008: WEB1000 Versions 3.1, 4.1 and 5.1, Picture Archiving and Communications systems…

FDA device recall · Class II · AGFA Corp.

Key facts

Recall number (Z-number) Z-1244-2008
Recall event 46384
Product WEB1000 Versions 3.1, 4.1 and 5.1, Picture Archiving and Communications systems (PACs), used in the acceptance, transfer, display, storage and digital processing of medical images.
Product code LLZ
Recalling firm AGFA Corp.
Recall class Class II
Status Terminated
Termination date Dec 9, 2010
510(k) numbers K022292, K040555, K050751, K053458
FEI number 3001236302

At a glance

  • 1–9 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)