Device recall

Z-0176-03: BrachyVision software, catalog #AL15521003, CD-ROM (set of four) packaged in…

FDA device recall · Class II · Varian Brachytherary Virginia

Key facts

Recall number (Z-number) Z-0176-03
Recall event 27629
Product BrachyVision software, catalog #AL15521003, CD-ROM (set of four) packaged in plastic sleeve and inserted into Varian Medical Systems Imaging Products Vision binder. Labeled in part ***Varian Medical Systems Inc. Oncology Systems***
Product code LNX
Recalling firm Varian Brachytherary Virginia
Recall class Class II
Status Terminated
Termination date Dec 15, 2003
510(k) numbers K992762
FEI number 3000206172

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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