Recall Radar

Pernod Ricard Usa recalls Copitas: contamination

May 31, 2023 · Pernod Ricard Usa Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct may exceed FDA guidance levels for leachable lead.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Pernod Ricard Usa
Location
New York, NY
Reported by FDA
May 31, 2023
Recall started
May 1, 2023
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Other foods
Reason type
Other contamination

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey
    Quantity: 177,000 copitas
    Codes: No codes. All product distributed since October 2022 is effected.

Where it was distributed

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

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Pernod Ricard Usa recalled 1 product, including Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey.

Why was it recalled?

Product may exceed FDA guidance levels for leachable lead.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

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…

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in other foods

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.