Boothwyn Pharmacy recalls Semaglutide 2.5 mg/mL injection (0.8 mL) due to subpotent drug risk. Affected units have batch code 03202025@9 BUD 07/18/2025. Consumers should check labels for this code.
Subpotent Drug
Boothwyn Pharmacy is recalling Semaglutide injections that may be subpotent, meaning they contain less active ingredient than intended. This could lead to reduced effectiveness in treating weight-related conditions. The recall is for specific batch numbers with the code 03202025@9 BUD 07/18/2025.
Subpotent drugs have less active ingredient than specified, which can reduce the medication's effectiveness. This means the treatment may not work as intended for weight management. However, the recall does not indicate a risk of serious injury or harm beyond reduced effectiveness.
People who purchased Semaglutide 2.5 mg/mL injection (0.8 mL) from Boothwyn Pharmacy with the batch code 03202025@9 BUD 07/18/2025 are affected. Those using the medication for weight management may be at risk of reduced effectiveness.
Check the label for the batch code 03202025@9 BUD 07/18/2025. The product is Semaglutide 2.5 mg/mL injection, 0.8 mL, sold by Boothwyn Pharmacy.
Look for the batch code 03202025@9 BUD 07/18/2025 on the label.
The recall is for subpotent drug risk, which means reduced effectiveness, not a risk of serious injury or harm.
Check the label for the batch code 03202025@9 BUD 07/18/2025. If it matches, contact Boothwyn Pharmacy for guidance.
The affected product is Semaglutide 2.5 mg/mL injection (0.8 mL) with batch code 03202025@9 BUD 07/18/2025, sold by Boothwyn Pharmacy.
We’ve drafted a message you can send Boothwyn Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0608-2025 — Boothwyn Pharmacy Boothwyn Pharmacy Hello, I own a Boothwyn Pharmacy that is covered by recall D-0608-2025 from Boothwyn Pharmacy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
