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