Basic Reset Inc.: Medical Device Recall in 2019 - (Recall #: Z-0348-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)

Product Classification:

Class II

Date Initiated: October 18, 2019

Date Posted: November 20, 2019

Recall Number: Z-0348-2020

Event ID: 84117

Reason for Recall:

FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.

Status: Completed

Product Quantity: 1257 units

Code Information:

All product distributed between November 7, 2017 to September 4, 2019

Distribution Pattern:

US, Puerto Rico, U.S. Virgin Islands, Canada, Mexico, Australia, PHILIPPINES, Greece, United Kingdom, Israel, Nigeria, Hungary, United Arab Emirates

Voluntary or Mandated:

FDA Mandated