Device recall

Z-0644-2007: BacT/VIEW C.30a Software update (P/N 514515-1) diagnostic data management…

FDA device recall · Class II · bioMerieux, Inc.

Key facts

Recall number (Z-number) Z-0644-2007
Recall event 37141
Product BacT/VIEW C.30a Software update (P/N 514515-1) diagnostic data management system, bioMerieux, Inc., P. O. Box 15969, Durham, NC 27704-0969 USA
Product code MDB
Recalling firm bioMerieux, Inc.
Recall class Class II
Status Terminated
Termination date Dec 8, 2009
510(k) numbers K903505, K934593, K954468, K981736
FEI number 3002769706

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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