Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug

Date: July 9, 2025
Company: Boothwyn Pharmacy LLC
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Boothwyn Pharmacy LLC directly.

Affected Products

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

Quantity: 642 vials

Why Was This Recalled?

Subpotent Drug

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Boothwyn Pharmacy LLC

Boothwyn Pharmacy LLC has 4 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report