RecallHawk
Class II Recall

CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN ALLERGY 10MG TABLETS 5 CT SKU 916116 GS ALLERGY LORATA

Family Dollar Stores, Llc.

Summary

The FDA issued a Class II for CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN ALLERGY 10MG TABL by Family Dollar Stores, Llc.. Reason: CGMP Deviations: product held outside appropriate storage temperature conditions..

Details

Source

Drug Recall

External ID

D-1451-2022

Action Date

2022-08-31

Status

Ongoing

Category

drug

Product Description

CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN ALLERGY 10MG TABLETS 5 CT SKU 916116 GS ALLERGY LORATADINE TABLET 30 CT SKU 916114 CLARITIN ALLERGY 10 MG TABLET 10 CT SKU 901655 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

Lot/Code Info: SKUs: 900834; 916116; 916114; 901655

Quantity Affected: Unknown

Reason for Recall

CGMP Deviations: product held outside appropriate storage temperature conditions.

Distribution

Nationwide within the United States

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-23

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 131 drug recalls issued in the same week, part of 272 drug-related FDA actions this month.

Family Dollar Stores, Llc. has 149 FDA actions in our database, including 149 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 (Family Dollar Stores, Llc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Family Dollar Stores, Llc. have FDA actions?

Family Dollar Stores, Llc. has 149 FDA actions in our database, including 149 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-1451-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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