PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: February 20, 2013 Initiated: October 10, 2012 #Z-0801-2013

Product Description

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.

Reason for Recall

The product may contain low level microbial contamination which could result in incorrect results.

Details

Recalling Firm
Remel Inc
Units Affected
10 units
Distribution
Distribution included the states of IL, IN and MI.
Location
Lenexa, KS

Frequently Asked Questions

What product was recalled?
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.. Recalled by Remel Inc. Units affected: 10 units.
Why was this product recalled?
The product may contain low level microbial contamination which could result in incorrect results.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 20, 2013. Severity: Moderate. Recall number: Z-0801-2013.