Harbin Jixianglong Biotech Co., Ltd.

FDA Regulatory Profile

Harbin Jixianglong Biotech Co., Ltd. appears in FDA public data with 2 recalls, 0 510(k) clearances, 1 FDA inspection, and 1 compliance action on record. Its most recent recall (D-0380-2026, Class II) was initiated on February 13, 2026.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
1
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0380-2026Class IISemaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106February 13, 2026
D-0379-2026Class IISemaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-February 13, 2026