Boothwyn Pharmacy recalled 642 vials of Semaglutide injection on July 9, 2025. The recall follows the discovery that the drug is subpotent. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Subpotent Drug
Consumers and healthcare providers should stop using this product immediately. Contact Boothwyn Pharmacy LLC or your healthcare provider for guidance. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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The recalled product is Semaglutide, 2.5 mg/mL injection, 2 mL vials. Model numbers include 03202025@5, 03202025@6, 03202025@7, and 03202025@8 with a BUD of 07/18/2025. The product was distributed nationwide in the U.S.
The recall is classified as Class II due to the subpotency of the drug. Subpotent medications may not provide the intended therapeutic effect, which can lead to inadequate treatment of conditions.
No specific injury or incident reports are mentioned. The recall is in response to the identified issue of subpotency.
Stop using the Semaglutide injection immediately. Contact Boothwyn Pharmacy LLC or your healthcare provider for further guidance.
For more information, visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0606-2025.
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