HIGH

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (High-Risk)

Boothwyn Pharmacy LLC issued a nationwide recall of 186 vials of Semaglutide 2.5 mg/mL injection, 0.8 mL, on July 9, 2025. The FDA enforcement report classifies the recall as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and follow guidance from Boothwyn Pharmacy or a healthcare provider.

Quick Facts at a Glance

Recall Date
July 9, 2025
Hazard Level
HIGH
Brand
Boothwyn Pharmacy
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, ELDERLY

Hazard Information

Subpotent Drug

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Boothwyn Pharmacy LLC or your healthcare provider for guidance. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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About This Product

Semaglutide is a prescription GLP-1 receptor agonist used for glycemic control in type 2 diabetes and obesity management.

Why This Is Dangerous

Subpotent drug may lead to reduced efficacy, potential poor disease management, and need for medical reassessment.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers and healthcare providers must halt use and await guidance; potential impact includes treatment disruption and need for alternative therapies.

Practical Guidance

How to identify if yours is affected

  1. Locate model number on the vial label: 03202025@9 BUD 07/18/2025
  2. Check packaging for lot numbers and dates if available
  3. Verify that the product is labeled Semaglutide 2.5 mg/mL injection, 0.8 mL

Where to find product info

FDA recall page D-0608-2025 for Boothwyn Pharmacy enforcement notice

What timeline to expect

Refund or replacement details to be issued by Boothwyn Pharmacy as recall progresses

If the manufacturer is unresponsive

  • Document all attempts to contact Boothwyn Pharmacy
  • File a consumer complaint with FDA if Boothwyn is unresponsive

How to prevent similar issues

  • Always verify drug potency with pharmacist before use
  • Watch for recall notices from pharmacies and manufacturers
  • Keep prescription records and batch/lot numbers secure

Documentation advice

Keep recall notification, packaging, receipts, and correspondence as records

Product Details

Model numbers: 03202025@9 BUD 07/18/2025. Quantity: 186 vials. Distribution: U.S. nationwide. Sold by Boothwyn Pharmacy. Recall date: 2025-07-09. Status: ACTIVE.

Reported Incidents

No specific injuries or incidents are listed in the provided data.

Key Facts

  • 186 vials recalled
  • Subpotent drug (Class II)
  • Recall date 2025-07-09
  • Active status as of 2025-09-10
  • Distribution nationwide
  • Model: 03202025@9 BUD 07/18/2025

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTELDERLYPREGNANTPREGNANT
Injury Types
ELECTRICALLACERATIONOTHER

Product Details

Model Numbers
03202025@9 BUD 07/18/2025
Affected States
ALL
Report Date
September 10, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (4 mL, 2.5 mg/mL)

Boothwyn Pharmacy recalls 648 vials of semaglutide 2.5 mg/mL injection nationwide after detecting subpotent potency. The recall involves products distributed across the U.S. and is classified as Class II with a high hazard level. Stop using the product and contact Boothwyn Pharmacy or a healthcare provider for guidance.

Boothwyn Pharmacy
Subpotent Drug
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