Oxus America, Inc.

FDA Regulatory Profile

Oxus America, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0768-2013, Class II) was initiated on January 14, 2013.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0768-2013Class IILi-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400. Also branded as ReliaJanuary 14, 2013