Copitas small ceramic cups recall
Recalled by Pernod Ricard Usa Inc · New York, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product may exceed FDA guidance levels for leachable lead.
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey
Quantity: 177,000 copitas
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No codes. All product distributed since October 2022 is effected.
Where it was sold
Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Florida Georgia Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri Mississippi North Carolina Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oregon Pennsylvania South Carolina South Dakota Tennessee Texas Washington Wisconsin
FDA's distribution note: 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
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Pernod Ricard Usa Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 1, 2023
- In FDA report of
- May 31, 2023
- Terminated
- Aug 21, 2023
- FDA recall number
- F-0953-2023 · event 92218
- Official record
- FDA enforcement report search