RecallHawk
Class II Recall

Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey

Pernod Ricard Usa Inc

Summary

The FDA issued a Class II for Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by by Pernod Ricard Usa Inc. Reason: Product may exceed FDA guidance levels for leachable lead..

Details

Source

Food Recall

External ID

F-0953-2023

Action Date

2023-05-31

Status

Terminated

Category

food

Product Description

Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey

Lot/Code Info: No codes. All product distributed since October 2022 is effected.

Quantity Affected: 177,000 copitas

Reason for Recall

Product may exceed FDA guidance levels for leachable lead.

Distribution

Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Washington DC, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, New Hampshire, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Washington, Wisconsin

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-01

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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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

How often does Pernod Ricard Usa Inc have FDA actions?

This is the only FDA action we have on record for Pernod Ricard Usa Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0953-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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