Mezzetta Recalls 32-Ounce Golden Greek Peperoncini Jars From Lot 720106 After Social Media Video Shows Possible Pest Contaminant

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Editorial Illustration via AI Share on Twitter Share on Facebook Share on Pocket G. L. Mezzetta Inc. is recalling one lot of its 32-ounce Mezzetta Golden Greek Peperoncini, Medium Heat, because the product may contain a pest contaminant, according to a company announcement posted by the FDA.

The company says it has received no reports of illness or injury. Anyone who has a jar from the affected lot is asked not to eat it.

The recall applies only to Mezzetta Golden Greek Peperoncini, Medium Heat, in 32-ounce jars, SKU 10106328, lot 720106. The company says that, based on the information currently available, no other Mezzetta products or lots are included.

The notice does not list a UPC, a best-by date, or where the lot code is printed on the jar. Customers who have questions about a Mezzetta product at home can contact the company at [email protected].

The recall followed a video posted online. “We’re aware of a video circulating on social media showing a potential pest contaminant in a jar of Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT, 32-ounce,” the company said. “We have contacted the consumer and have moved quickly to investigate the situation and initiate a voluntary recall.”

A Houston Chronicle headline reported that a TikTok user claimed to have found a dead mouse in a jar. Mezzetta has not identified the type of pest, and other coverage, including a report by NTD, described the video only as appearing to show a pest.

Mezzetta describes the action as a limited voluntary recall. The company says it has “identified the customers that received product from the recalled lot and are working directly with them to isolate and remove the affected product from sale.” It has not named the stores or states involved.

The company also says it has asked to retrieve and examine the product from the original consumer report and is “reviewing the relevant production, sanitation and food-safety records as part of our ongoing investigation.” According to the FDA page, the firm updated the product information on Sept. 26 to accurately reflect the recalled item. Some early coverage referred to the product as Mezzetta Greek Peppers.

The company’s instruction is direct: “If you believe you have a 32 oz. jar of Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT from lot 720106, please do not consume the product and contact Mezzetta at [email protected] for assistance.”

The notice does not list a company phone number or describe a refund process. Mezzetta says it is coordinating with regulators and will update its notice if the scope of the recall or its guidance to consumers changes.

The company notice does not include a recall classification. The FDA assigns a class after its own hazard review, and lists recalls in its weekly Enforcement Report, which may also show a recall as pending classification.

Under FDA recall definitions, a Class I recall involves a reasonable probability of serious adverse health consequences or death. A Class II recall covers products that may cause temporary or medically reversible health problems, or where the chance of serious harm is remote. A Class III recall covers products “not likely to cause adverse health consequences.”

Consumers can report a problem with an FDA-regulated food through the agency’s online consumer complaint reporting system or by calling 1-888-INFO-FDA (1-888-463-6332).

Which product is recalled? Mezzetta Golden Greek Peperoncini, Medium Heat, in 32-ounce jars from lot 720106, SKU 10106328. The company says no other Mezzetta products or lots are included.

Why was it recalled? A video on social media appeared to show a pest contaminant in a jar. Mezzetta has not identified the type of pest.

Has anyone gotten sick? The company says it has received no reports of illness or injury.

What should I do if I have a jar from the recalled lot? Do not eat it, and contact Mezzetta at [email protected] for assistance.

Has the FDA classified the recall? The company notice does not include a classification. The FDA lists recall classes in its weekly Enforcement Report.