Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PR
Summary
The FDA issued a Class II for Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AM by G L Mezzetta Inc. Reason: Potential contamination with foreign objects: mice..
Details
Source
Food Recall
External ID
H-0007-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
Product Description
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PRODUCT OF GREECE UPC: 073214003280
Lot/Code Info: Lots: 720106. Best if used by: July 2029.
Quantity Affected: 7,497 cases (6 units/case)
Reason for Recall
Potential contamination with foreign objects: mice.
Distribution
Domestic: AZ, CA, CO, GA, IA, ID, IL, IN, MI, MN, MO, NC, OH, OK, OR, PA, SD, TX, UT, VA, WA, WI. Foreign: Not applicable.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-19
Company
American Canyon, CA
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 35 food recalls issued in the same week, part of 92 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 (G L Mezzetta Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does G L Mezzetta Inc have FDA actions?
This is the only FDA action we have on record for G L Mezzetta Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0007-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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