PlainRecalls
FDA Drug Moderate Class II Ongoing

Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy

Reported: September 10, 2025 Initiated: July 9, 2025 #D-0609-2025

Product Description

Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy

Reason for Recall

Subpotent Drug

Details

Recalling Firm
Boothwyn Pharmacy LLC
Units Affected
648 vials
Distribution
U.S. Nationwide
Location
Kennett Square, PA

Frequently Asked Questions

What product was recalled?
Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy. Recalled by Boothwyn Pharmacy LLC. Units affected: 648 vials.
Why was this product recalled?
Subpotent Drug
Which agency issued this recall?
This recall was issued by the FDA Drug on September 10, 2025. Severity: Moderate. Recall number: D-0609-2025.