RecallHawk
Class I Recall

Backcountry Dried Apricots 9ounce plastic bag 12 packages per case

Lipari Foods Operating Company, LLC.

Summary

The FDA issued a Class I for Backcountry Dried Apricots 9ounce plastic bag 12 packages per case by Lipari Foods Operating Company, LLC.. Reason: Sulfites not disclosed on labeling.

Details

Source

Food Recall

External ID

F-0795-2021

Action Date

2021-08-04

Status

Terminated

Category

food

Product Description

Backcountry Dried Apricots 9ounce plastic bag 12 packages per case

Lot/Code Info: Best By Dates: 07/2021, 11/2021, 12/2021 Lot No. 440021117 Product No. 276033

Quantity Affected: 86 cases

Reason for Recall

Sulfites not disclosed on labeling

Distribution

Distributed to retail locations in the following states: AL, FL, GA, ID, IL, IN, KS, KY, MI, MO, NC, OH, PA, TN, UT, VA, WI WV.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-07-16

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 31 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Lipari Foods Operating Company, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lipari Foods Operating Company, LLC. have FDA actions?

Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0795-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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