National Biological Corp recalls Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototh…

Recall date

January 27, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1683-2017

FDA classification

Class II

Brand / firm

National Biological Corp

Sold / distributed

Worldwide distribution. US states: IA, IL, MI, NY, PA, and WI. Country: Jordan. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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