RecallHawk
Class II Recall

Global Care Antibacterial Hand Sanitizer Alcohol Etilico 70% Original, 1 Gallon (128 FL OZ) 3785.41 mL, Dist. by Target

Frenda Corporation

Summary

The FDA issued a Class II for Global Care Antibacterial Hand Sanitizer Alcohol Etilico 70% Original, 1 Gallon by Frenda Corporation. Reason: cGMP Deviations.

Details

Source

Drug Recall

External ID

D-0259-2023

Action Date

2023-02-08

Status

Terminated

Category

drug

Product Description

Global Care Antibacterial Hand Sanitizer Alcohol Etilico 70% Original, 1 Gallon (128 FL OZ) 3785.41 mL, Dist. by Target Price, Inc. Catano, PR, UPC 8 70373 01326 2

Lot/Code Info: Lot: C013121

Quantity Affected: 124 bottles

Reason for Recall

cGMP Deviations

Distribution

Puerto Rico

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-15

Company

Frenda Corporation

Trujillo Alto, PR

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

Frenda Corporation has 7 FDA actions in our database, including 7 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 (Frenda Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Frenda Corporation have FDA actions?

Frenda Corporation has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0259-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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