FDAFDA · Food and drugs·Recall number Z-0801-2013
The product is a lyophilized growth supplement for use with dehydrated culture media to prepare BCYE Medium used for isolation of Legionellae from clinical and environmental samples.
Published February 20, 2013 · Recall initiated: October 10, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The product may contain low level microbial contamination which could result in incorrect results.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Remel Inc
- Distributor
- Distribution included the states of IL, IN and MI.
- Lot
- Lot 1175209
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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