Fresh Seasons Kitchen Power Pack. Fresh grapes, mild cheddar cheese, hard-boiled egg, whole wheat flatbread & Peanut Bu
Summary
The FDA issued a Class I for Fresh Seasons Kitchen Power Pack. Fresh grapes, mild cheddar cheese, hard-boile by Taher, Inc.. Reason: Product contains .75 oz container of Jif Peanut Butter that is recalled due to Salmonella contamination..
Details
Source
Food Recall
External ID
F-1319-2022
Action Date
2022-06-29
Status
Terminated
Category
food
Product Description
Fresh Seasons Kitchen Power Pack. Fresh grapes, mild cheddar cheese, hard-boiled egg, whole wheat flatbread & Peanut Butter. ID# HP-981 UPC 10106-02165. Keep Refrigerated. Labeled with either 1. Manufactured for Holiday Commissary, 6890 Shingle Creek Parkway, Brooklyn Center, MN 55430, or 2. Taher, Inc., 10205 51st Ave. N., Plymouth, MN 55442.
Lot/Code Info: Lots: 135, 136, 137, 138, 140, 142 Exp Dates from 5/24/2022 to 5/31/2022
Quantity Affected: 2735 units
Reason for Recall
Product contains .75 oz container of Jif Peanut Butter that is recalled due to Salmonella contamination.
Distribution
MN
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-23
Company
Plymouth, MN
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 78 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Taher, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Taher, Inc. have FDA actions?
This is the only FDA action we have on record for Taher, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1319-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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