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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Boothwyn Pharmacy Semaglutide and Fluorescein Recalled for Subpotency

Agency Publication Date: August 29, 2025
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Summary

Boothwyn Pharmacy LLC is recalling approximately 1,484 vials of Semaglutide injections and Fluorescein 2% ophthalmic solution. The recall was initiated because these products are subpotent, meaning they contain less active medication than indicated on the label. Semaglutide is a medication used for weight management and blood sugar control, while Fluorescein is a dye used by eye care professionals during ophthalmic procedures.

Risk

Using subpotent medication may lead to decreased effectiveness of the treatment, potentially failing to control the medical conditions for which they were prescribed. No specific injuries or adverse health effects have been reported in the recall data.

What You Should Do

  1. The recalled products are Semaglutide 2.5 mg/mL injections (available in 0.8 mL, 2 mL, and 4 mL vials) and Fluorescein 2% Ophth (3 mL vials) sold under the Boothwyn Pharmacy brand.
  2. Check your medication for the following lot numbers: 03202025@2, 03202025@3, 03202025@4, 03202025@5, 03202025@6, 03202025@7, 03202025@8, and 03202025@9 with a Best Use Date (BUD) of 07/18/2025; or lot 06092025@23 with a BUD of 09/09/2025.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Boothwyn Pharmacy at 800-476-7496 for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Semaglutide 2.5 mg/mL injection (2 mL)by Boothwyn Pharmacy
Variants: 2.5 mg/mL, Injection
Lot Numbers:
03202025@5 (BUD 07/18/2025)
03202025@6 (BUD 07/18/2025)
03202025@7 (BUD 07/18/2025)
03202025@8 (BUD 07/18/2025)

Quantity: 642 vials; Recall #: D-0606-2025

Product: Fluorescein 2% Ophth (3 mL)by Boothwyn Pharmacy
Variants: 2%, Ophthalmic Solution
Lot Numbers:
06092025@23 (BUD 09/09/2025)

Quantity: 8 vials; Recall #: D-0607-2025

Product: Semaglutide 2.5 mg/mL injection (0.8 mL)by Boothwyn Pharmacy
Variants: 2.5 mg/mL, Injection
Lot Numbers:
03202025@9 (BUD 07/18/2025)

Quantity: 186 vials; Recall #: D-0608-2025

Product: Semaglutide 2.5 mg/mL injection (4 mL)by Boothwyn Pharmacy
Variants: 2.5 mg/mL, Injection
Lot Numbers:
03202025@2 (BUD 07/18/2025)
03202025@3 (BUD 07/18/2025)
03202025@4 (BUD 07/18/2025)

Quantity: 648 vials; Recall #: D-0609-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97202
Status: Active
Manufacturer: Boothwyn Pharmacy LLC
Sold By: Boothwyn Pharmacy
Manufactured In: United States
Units Affected: 4 products (642 vials; 8 vials; 186 vials; 648 vials)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.