RecallHawk
Class II Recall

70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 5

Tsm Brands LLC

Summary

The FDA issued a Class II for 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML b by Tsm Brands LLC. Reason: Labeling - product contains undeclared ethyl alcohol.

Details

Source

Drug Recall

External ID

D-0635-2022

Action Date

2022-03-09

Status

Ongoing

Category

drug

Product Description

70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 540 Equinox LN, Manalapan, NJ 07726, www.tsmbrands.com, Made in Turkey, UPC 868275965765

Lot/Code Info: Lot#: 39,40,41,42,43,44 and 45

Quantity Affected: 1.186.800 bottles

Reason for Recall

Labeling - product contains undeclared ethyl alcohol

Distribution

USA Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-07

Company

Tsm Brands LLC

Manalapan, NJ

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

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

How often does Tsm Brands LLC have FDA actions?

Tsm Brands 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-0635-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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