RecallHawk
Class II Recall

Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way,

Washington Homeopathic Products, Inc.

Summary

The FDA issued a Class II for Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeo by Washington Homeopathic Products, Inc.. Reason: cGMP deviations.

Details

Source

Drug Recall

External ID

D-1130-2022

Action Date

2022-06-22

Status

Terminated

Category

drug

Product Description

Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411,

Lot/Code Info: Lot # 20332, 20333

Quantity Affected: 7 glass amber bottles

Reason for Recall

cGMP deviations

Distribution

Product was distributed USA nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-13

Company

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

Washington Homeopathic Products, Inc. has 57 FDA actions in our database, including 57 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 (Washington Homeopathic Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Washington Homeopathic Products, Inc. have FDA actions?

Washington Homeopathic Products, Inc. has 57 FDA actions in our database, including 57 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-1130-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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