FDAJanuary 27, 2017device

Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The wiring may allow the lamps to turn on with the key switch rather than the timer.

What to do

FDA enforcement status: Terminated

Brands named

national biologicalnational

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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