Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
The hazard: Potency, impurity or stability failure
An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
What the notice says: Subpotent Drug
Why it matters: The product failed a specification test: it may contain more or less active ingredient than the label states, carry an impurity, or degrade before its expiry date. A sub-potent dose can leave a condition untreated; a super-potent one can cause an overdose.
Symptoms and when to call a doctor
The risk depends entirely on the drug. For a medicine where dose matters closely — a blood thinner, an anti-epileptic, a thyroid or heart medicine, insulin — talk to your prescriber before changing anything. Seek urgent care if you have symptoms that suggest too much drug, or if the condition the medicine controls starts breaking through.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- D-0609-2025
- Published
- September 10, 2025
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Boothwyn Pharmacy LLC
- Product type
- Prescription & OTC drugs
- Units affected
- 648 vials
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- 03202025@2, 03202025@3 and 03202025@4 BUD 07/18/2025
Products covered by this recall
Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy
Check your product
The notice names 2 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Package size
Match the net weight or the piece count on the front of the pack.
- 2.5 mg
- 4 mL
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Potency
Boothwyn Pharmacy LLC — An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
- Check the lot number on your pack against the codes listed above before you do anything else.
- Call your prescriber or pharmacist and ask whether to swap the lot, re-test, or change nothing.
- Keep the carton and the leaflet — the lot number is usually printed only on the outer pack.
- Report any change in how the medicine is working to FDA MedWatch, which is where most of these signals originate.
What the company owes you
A recalled medicine is the manufacturer’s cost to carry, not yours or your pharmacist’s.
- The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
- Ask the pharmacy to handle the claim where they can — they process recall returns in bulk and it saves you the correspondence.
- Keep the carton, the leaflet and the pharmacy label together until the claim is closed.
- Costs beyond the price of the medicine need to go to the company directly, in writing, with the recall number quoted.
Company contact: Boothwyn Pharmacy LLC — 221 Gale Ln, Kennett Square, PA, 19348
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Boothwyn Pharmacy LLC prescription & otc drugs recalled?
Subpotent Drug Subpotent Drug
How do I know if I have the recalled product?
The notice does not publish package codes for this recall. Compare the product name, size and the purchase window against the official FDA — Drug enforcement record, and contact the company if you are unsure.
What should I do with it right now?
Check the lot number on your pack against the codes listed above before you do anything else.
Can I get my money back?
The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
-
Class III · 1+ years ago
Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496 recall: Subpotent Drug
Subpotent Drug
-
Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
-
Class II · 11 days ago
K.C. Pharmaceuticals, Inc. Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
-
Class II · 11 days ago
Carolina Infusion, LLC Quad-Mix Injectable, Packaged in single-use dosage syringes recall: Lack of Assurance of Sterility: Related to processing equipment used
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
-
Class II · 11 days ago
Carolina Infusion, LLC Tirzepatide/Cyanocobalamin 26/2 MG/ML Injectable recall: Lack of Assurance of Sterility: Related to formulation using bacteriostic
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.