Diamedix Is-CMV IgG Test Kit Recalled for Incorrect Substrate
Diamedix Corporation is recalling 150 Is-CMV IgG Test Kits because the product contained an incorrect substrate.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or hospitalizations, fitting the criteria for a moderate severity score.
Plain-English summary
Diamedix Corporation is recalling 150 units of the Diamedix Is-CMV IgG Test Kit. The recall was initiated because the product contained an incorrect substrate.
The affected product is identified by Catalog # 720-320, Lot # 10105, and an expiration date of January 31, 2016. The kits were distributed in Arizona, California, Florida, Georgia, Kentucky, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New York, Ohio, Oklahoma, Oregon, Tennessee, Texas, Virginia, Wisconsin, and Puerto Rico.
Consumers who have this product should stop using it and contact Diamedix Corporation for further instructions.
The recalled product
- Product
- Diamedix Is-CMV IgG Test Kit
- Manufacturer
- Diamedix Corporation
- Hazard
- Affected units
- 150
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Catalog # 720-320 Lot # 10105 Expiration Date January 31
- 2016
Distribution
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