FDA recall record

Cutera brand truSculpt infrared System (optional), Massager, Vacuum, radio frequency induced recall — FDA Z-0427-2014

Cutera received two adverse events associated with the edge of the electrode, when it was pressed against neck skin over the thyroid cartilage and due to…

Class IIclassification
Z-0427-2014official record ID
Dec 18, 2013report date

Recall record at a glance

Official recordZ-0427-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCutera, Inc.
Report dateDec 18, 2013
Recall initiation dateOct 16, 2013
Quantity451
LocationBrisbane, CA, United States

Official product description

Cutera brand truSculpt infrared System (optional), Massager, Vacuum, radio frequency induced heat, Product is manufactured and distributed by Cutera, Inc., Brisbane, CA The truSculpt massage device is intended to provide a temporary reduction in the appearance of cellulite. The truSculpt infrared (optional) and RF energies are intended to provide topical heating for the purpose of elevating tissue temperature for the treatment of selected medical conditions such as relief of pain, muscle spasms, and increase in local circulation.

Why the product was recalled

Cutera received two adverse events associated with the edge of the electrode, when it was pressed against neck skin over the thyroid cartilage and due to the absence of adequate underlying conductive tissue, increased skin heating occurred. Both patients developed linear welts and blisters consistent with partial thickness thermal burns to the skin.

Distribution information

Worldwide Distribution - USA (nationwide) and Internationally to Canada

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.

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