RecallHawk
Class III Recall

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Healt

Amerisource Health Services LLC

Summary

The FDA issued a Class III for HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, by Amerisource Health Services LLC. Reason: Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point..

Details

Source

Drug Recall

External ID

D-0039-2024

Action Date

2023-10-11

Status

Terminated

Category

drug

Product Description

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11

Lot/Code Info: Lot#: 1007002, Exp 12/31/2023

Quantity Affected: 3,344 cartons

Reason for Recall

Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.

Distribution

Nationwide in the USA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-09-01

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 59 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Amerisource Health Services LLC has 46 FDA actions in our database, including 46 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Amerisource Health Services LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Amerisource Health Services LLC have FDA actions?

Amerisource Health Services LLC has 46 FDA actions in our database, including 46 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0039-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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