WhichRecall
Class IIReported 2025-10-15

Semaglutide for Injection, a) 20 mg b) 20 mg/mL, 10 mL Multi-Dose Vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness, 20 mg, 10mL vial lyophilized.

Recalled by GenoGenix LLC

Reason for Recall

Lack of Assurance of Sterility

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Recall Number
D-0091-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-07-30
Reported
2025-10-15
Distribution
US Nationwide.
Code Info
Lot#: GG021125-001, GG031125-017, within expiry.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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