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.
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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 FDA.gov:
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 FDA.gov
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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.