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Home > Recalled Products > Pet Care Products > Defect > Jurox Alfaxan Unpreserved, An Intravenous Injectable Anaesthetic

Recall: Jurox Alfaxan Unpreserved, An Intravenous Injectable Anaesthetic


On 2019-04-24, the FDA announced that Jurox is conducting a recall on Alfaxan Unpreserved, An Intravenous Injectable Anaesthetic due to a possible . The recalled products were sold under the brand name(s) Jurox during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 pet care products recalls due to potential defect, including poultry feed, and more.

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Alfaxan Unpreserved, an Intravenous Injectable Anaesthetic, Label
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Company Contact Information:

Name: Jurox

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Detailed Recall Information

Regions Where Sold: Nationwide

Product Description: Alfaxan Unpreserved, an Intravenous Injectable Anaesthetic

Brand Name(s): Jurox

Reason for Recall: Defect

Official Recall Date: 2019-04-24


Additional information provided by the

The presence of the aluminum phosphate precipitate presents a potential risk that intravascular (I.V.) injection of product containing this precipitate could result in blood vessel inflammation, and formation of blood clots or embolisms, which can be life threatening. Read More.

More information may be available at

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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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