Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to Device was shipped without a Unique Device Identification...
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, used for the temporary relief of knee pain.
Quantity: 41 units
Why Was This Recalled?
Device was shipped without a Unique Device Identification (UDI) label.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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