RecallHawk
Class II Recall

American Gourmet Saladitos (Dried Salted Plums) 1.5 oz. package UPC: 1578600104

American Gourmet

Summary

The FDA issued a Class II for American Gourmet Saladitos (Dried Salted Plums) 1.5 oz. package UPC: 1578600104 by American Gourmet. Reason: California Department of Public Health sampled product and found it to contain high levels of lead..

Details

Source

Food Recall

External ID

F-0830-2022

Action Date

2022-03-16

Status

Terminated

Category

food

Product Description

American Gourmet Saladitos (Dried Salted Plums) 1.5 oz. package UPC: 1578600104

Lot/Code Info: Lot 211203; Sell by 12/03/2022

Quantity Affected: 193 lbs

Reason for Recall

California Department of Public Health sampled product and found it to contain high levels of lead.

Distribution

CA only

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-07

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 92 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 (American Gourmet) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does American Gourmet have FDA actions?

This is the only FDA action we have on record for American Gourmet in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0830-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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