National Biological Corp: Medical Device Recall in 2017 - (Recall #: Z-1683-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 27, 2017

Date Posted: April 5, 2017

Recall Number: Z-1683-2017

Event ID: 76725

Reason for Recall:

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

Status: Terminated

Product Quantity: 7 units

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.

Voluntary or Mandated:

Voluntary: Firm initiated