RecallHawk
Class III Recall

Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, 1250 mL (42 fl oz.), Manufactured for

Woodbine Products Co Inc

Summary

The FDA issued a Class III for Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scen by Woodbine Products Co Inc. Reason: Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label..

Details

Source

Drug Recall

External ID

D-0006-2023

Action Date

2022-10-12

Status

Terminated

Category

drug

Product Description

Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, 1250 mL (42 fl oz.), Manufactured for: Triple S, 800-323-2251, Made in USA, NDC 11429-1010-8

Lot/Code Info: Lot #: VDAF017, Exp 4/24; VDAF018, Exp 5/24

Quantity Affected: 595 cases (4 bottles per case)

Reason for Recall

Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.

Distribution

NC

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-30

Company

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

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 (Woodbine Products Co Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Woodbine Products Co Inc have FDA actions?

This is the only FDA action we have on record for Woodbine Products Co Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0006-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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