Boothwyn Pharmacy recalled 648 vials of Semaglutide injection on July 9, 2025. The product is subpotent and poses a high hazard risk. Consumers should stop using the product immediately and contact their healthcare provider.
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
The recall pertains to Semaglutide, 2.5 mg/mL injection, packaged in 4 mL vials. Models include 03202025@2, 03202025@3, and 03202025@4 with a use-by date of July 18, 2025. The product was distributed nationwide in the U.S.
The recalled Semaglutide injection is classified as subpotent. This could lead to inadequate treatment for conditions it is prescribed for, potentially resulting in serious health risks.
No injuries or incidents have been reported at this time. The potential for health complications remains a concern due to the drug's subpotency.
Stop using the recalled Semaglutide injection immediately. Contact Boothwyn Pharmacy LLC or your healthcare provider for guidance on alternative treatments.
For more information, contact Boothwyn Pharmacy at their official channels or visit their FDA recall page.
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