Technological Medical Advancements LLC recalls Diowave Laser System, REF: Diowave 250W
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local…
Read the official notice →- Date
- 2026-05-20
- Country
- United States
- Brand
- Technological Medical Advancements LLC
- Product
- Diowave Laser System, REF: Diowave 250W
- Classification
- Class II
- Units
- US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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