Acumedia Manufacturers, Inc.: Medical Device Recalls in 2018

According to to data from the FDA, there were 2 medical device recalls made by Acumedia Manufacturers, Inc. in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.
• Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter spp. In a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.