Class II

Medical Device Recall: Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

Parker Laboratories, Inc. · March 22, 2024

Reason for Recall

Product demonstrates low viscosity.

Distribution

Worldwide distribution - US Nationwide in the states of CA, CO, FL, GA, IL, MD, MI, MN, NC, NE, NY, OH, PA, SC, & TX. The countries of AU, CA, OM, & SA.

States Affected

NATIONWIDE

Quantity Affected

217 cases (1,085 Inner Boxes; 10,850 Eaches)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1604-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.