US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 9, 2025 (14 months ago)

Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug

What was recalled

Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy

Recalling firm
Boothwyn Pharmacy LLC
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0608-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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