Boothwyn Pharmacy recalls Semaglutide 2.5 mg/mL injection (2mL) due to subpotent drug levels. Affected lots: 03202025@5-8, batched until July 2025. No specific remedy stated in recall notice.
Subpotent Drug
Boothwyn Pharmacy is recalling Semaglutide 2.5 mg/mL injections (2mL) because they contain subpotent drug levels. This means the medication may not work as intended for weight management. Consumers should check their product labels to see if they have the affected lots.
Subpotent drugs have lower active ingredient concentrations than intended, which can lead to reduced effectiveness. This means the medication may not work as well for weight management as it should. However, this does not pose a safety risk to the user.
People who purchased Semaglutide 2.5 mg/mL injection (2mL) from Boothwyn Pharmacy between 2020 and 2025 are likely affected. Those using the medication for weight management are most at risk of reduced effectiveness.
Check the product label for the lot numbers 03202025@5, 03202025@6, 03202025@7, or 03202025@8. The product was manufactured with a batch expiration date of July 18, 2025.
Look for lot numbers 03202025@5 through 03202025@8 on the Semaglutide 2.5 mg/mL injection (2mL) label.
No, this recall is for reduced effectiveness, not safety risks. The medication may not work as intended but does not cause harm.
The recall notice does not specify a remedy. Check the product label for lot numbers to see if it's affected.
The product was manufactured with a batch expiration date of July 18, 2025.
We’ve drafted a message you can send Boothwyn Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0606-2025 — Boothwyn Pharmacy Boothwyn Pharmacy Hello, I own a Boothwyn Pharmacy that is covered by recall D-0606-2025 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.
