RecallHawk
Class II Recall

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

Boothwyn Pharmacy LLC

Summary

The FDA issued a Class II for Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy by Boothwyn Pharmacy LLC. Reason: Subpotent Drug.

Details

Source

Drug Recall

External ID

D-0606-2025

Action Date

2025-09-10

Status

Ongoing

Category

drug

Product Description

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

Lot/Code Info: 03202025@5, 03202025@6, 03202025@7, 03202025@8 BUD 07/18/2025

Quantity Affected: 642 vials

Reason for Recall

Subpotent Drug

Distribution

U.S. Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2025-07-09

Company

Boothwyn Pharmacy LLC

Kennett Square, PA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 46 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Boothwyn Pharmacy LLC has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Boothwyn Pharmacy LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Boothwyn Pharmacy LLC have FDA actions?

Boothwyn Pharmacy LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0606-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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