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Recall Observatory FDA recall evidence

Device product

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

Z-1683-2017

January 27, 2017

Class II

Product summary

Firm
National Biological Corp
Event
Event 76725
Status
Terminated
Classification
Class II
Quantity
7 units
Official record key
device-enforcement:Z-1683-2017

Official wording

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

Code information: Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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