Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

TLC-2000 Therapeutic Medical Laser System Power Pack Recalled by Theralase Inc. Due to Power Pack (component) was shipped with an internal...

Date: September 26, 2019
Company: Theralase Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Theralase Inc. directly.

Affected Products

TLC-2000 Therapeutic Medical Laser System Power Pack, Model Number TLC-2002

Quantity: 202 units

Why Was This Recalled?

Power Pack (component) was shipped with an internal battery pack tested to UN-38.3, UL-2054 and IEC-62133 (2nd Edition) standards; however, not tested to IEC-60601-1-2 (3rd edition) standards

Where Was This Sold?

U.S.A.; Australia, Bahrain, Canada, Hong Kong Province of China, Jordan, Mexico, Pakistan, Philippines, Thailand, Romania

About Theralase Inc.

Theralase Inc. has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report