Recall RadarSemaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-0…
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Harbin Jixianglong Biotech Co., Ltd. — Haerbin, N/A
- Severity
- Class II — moderate
- Reported
- March 11, 2026
- Quantity
- N/A
- Recall number
- D-0379-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide within the United States
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