CLASS II ONGOING Drug recall · Reported 10 Sep 2025 · FDA Enforcement Report

Semaglutide, 5 mg/mL injection, Boothwyn Pharmacy recalled

Boothwyn Pharmacy is recalling Semaglutide, 5 mg/mL injection, Boothwyn Pharmacy, distributed nationwide in the US. The recall was initiated on 9 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes03202025@5, 03202025@6, 03202025@7, 03202025@8 BUD 07/18/2025
Quantity recalled642 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0606-2025
FDA event ID
97202
Recalling firm
Boothwyn Pharmacy, Kennett Square, PA
Classification
Class II
Status
Ongoing
Recall initiated
9 Jul 2025
FDA classified
29 Aug 2025
Reported
10 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Potency & Assay

Timeline

9 Jul 2025Recall initiated by company
29 Aug 2025Classified by FDA+51 days
10 Sep 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent Drug

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy

Where it was distributed

U.S. Nationwide

Nationwide

Questions about this recall

Is Semaglutide, 5 mg/mL injection, Boothwyn Pharmacy recalled?

Yes. Boothwyn Pharmacy recalled Semaglutide, 5 mg/mL injection, Boothwyn Pharmacy on 9 Jul 2025. The recall is Class II and its status is Ongoing. Recall number D-0606-2025.

Why was it recalled?

Subpotent Drug

Which lots are affected?

03202025@5, 03202025@6, 03202025@7, 03202025@8 BUD 07/18/2025

Where was it sold?

U.S. Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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