Drug & medication recalls Moderate risk

Boothwyn Pharmacy LLC recalls Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy

Recall date
July 9, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
D-0606-2025
FDA classification
Class II
Brand / firm
Boothwyn Pharmacy LLC
Sold / distributed
U.S. Nationwide

Why it was recalled

Subpotent Drug

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy

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