Z-1683-2017 Class II Terminated
FDA device recall Z-1683-2017 was initiated by National Biological Corp on January 27, 2017 and is designated Class II. Reason for recall: The wiring may allow the lamps to turn on with the key switch rather than the timer. The recall status is terminated (terminated February 8, 2019). Affected quantity: 7 units.
Recall Details
- Product Type
- Devices
- Report Date
- April 5, 2017
- Initiation Date
- January 27, 2017
- Termination Date
- February 8, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7 units
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.
Reason for Recall
The wiring may allow the lamps to turn on with the key switch rather than the timer.
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.
Code Information
Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869