Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
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
Company
Warren, MI
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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