RecallHawk
Class II Recall

Pyridoxine HCL (B6) Injection Solution, 100mg/mL, 30 mL Sterile Multiple-Dose Vial, For IM or IV use only, RX Only, Comp

Empower Pharmacy

Summary

The FDA issued a Class II for Pyridoxine HCL (B6) Injection Solution, 100mg/mL, 30 mL Sterile Multiple-Dose Vi by Empower Pharmacy. Reason: Lack of Assurance of Sterility.

Details

Source

Drug Recall

External ID

D-0663-2024

Action Date

2024-10-02

Status

Terminated

Category

drug

Product Description

Pyridoxine HCL (B6) Injection Solution, 100mg/mL, 30 mL Sterile Multiple-Dose Vial, For IM or IV use only, RX Only, Compounded by: Empower Pharmacy 5980 W Sam Houston Pkwy N Ste 300, Houston, TX 77041 NDC 72627-2424-1.

Lot/Code Info: Product lot number: 609763 Beyond Use Date: 04/18/2025

Quantity Affected: 450

Reason for Recall

Lack of Assurance of Sterility

Distribution

Nationwide

Recall Initiated: 2024-09-05

Company

Empower Pharmacy

Houston, TX

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 31 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

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 (Empower Pharmacy) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Empower Pharmacy have FDA actions?

This is the only FDA action we have on record for Empower Pharmacy in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0663-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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