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Recalls & Warnings January 21, 2018 Joint Supplement Recalled for Salmonella Risk On January 21, 2018, Arthri-D, LLC announced a recall of its joint pain supplement, Arthri-D (120 count), due to possible Salmonella contamination

All dosing figures describe a documented research protocol, not clinical guidance

Developed by BioSpecifics Technologies Corporation and marketed as XIAFLEX in the U.S

Reconstitution process CJC-1295 typically comes as a lyophilized (freeze-dried) powder

Neuroreport 31 , 12831288 (2020)

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