FDA recall record

Ra Medical Systems Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 recall — FDA Z-1631-2020

At doses of less than 100 mJ, in custom and auto repeat modes, a software error in the excimer laser phototherapy system causes the device to fail to…

Class IIclassification
Z-1631-2020official record ID
Apr 8, 2020report date

Recall record at a glance

Official recordZ-1631-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRa Medical Systems, Inc.
Report dateApr 8, 2020
Recall initiation dateAug 23, 2019
Quantity10
LocationCarlsbad, CA, United States

Official product description

Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the skin disorders psoriasis, vitiligo, atopic dermatitis, and leukoderma using phototherapy. The excimer laser system produces collimated 308 nm radiation, within the invisible region of the electromagnetic spectrum. The UV radiation falls within the range of ultraviolet B (UVB), which is used to treat photo-responsive skin disorders.

Why the product was recalled

At doses of less than 100 mJ, in custom and auto repeat modes, a software error in the excimer laser phototherapy system causes the device to fail to cease firing as long as the foot pedal or handpiece switch is depressed. This malfunction can cause overtreatment, which could result in strong erythema, and possibly cause blisters.

Distribution information

U.S. Nationwide distribution in the states of CA, FL, OR, MS, NY.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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