Drug recall

Bioplex Copper 10%, a feed premix, packaged in 25kg bags.

FDA recall event 38001 · Class III · Alltech Inc

Key facts

Event ID 38001
Recall numbers V-056-2007, V-057-2007, V-058-2007, V-059-2007, V-060-2007, V-061-2007, V-062-2007, V-063-2007, V-064-2007, V-065-2007, V-066-2007, V-067-2007 and 1 more
Recalling firm Alltech Inc
Product type Veterinary
Products Bioplex Copper 10%, a feed premix, packaged in 25kg bags., Bioplex mix Woody's, a feed premix packaged in 25kg bags., Bioplex Quadra, a feed premix packaged in 25kg bags., Bioplex/Selplex, a feed premix packaged in 25kg bags., Bioplex ZMC 842 + Co, a feed premix packaged in 25kg bags. and 8 more
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Bioplex Copper 10%, a feed premix, and premixes containing Bioplex Copper, were made using copper sulfate pentahydrate that was contaminated with dioxin like PCBs.
Initiation date Mar 26, 2007
Termination date Feb 7, 2012
City Nicholasville
State KY
Country United States
FEI number 1037117

At a glance

  • 10–99 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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