RecallHawk
Class I Recall

Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in a clear plastic hinged container, Net wt. 14oz. UPC 0 227862

Albertsons Companies LLC

Summary

The FDA issued a Class I for Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in a clear plastic hing by Albertsons Companies LLC. Reason: Undeclared peanut and soy..

Details

Source

Food Recall

External ID

F-0955-2023

Action Date

2023-05-31

Status

Terminated

Category

food

Product Description

Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in a clear plastic hinged container, Net wt. 14oz. UPC 0 227862 70500 7. Distributed by Safeway Inc. Pleasanton, CA 94588. The Oatmeal Raisin scale label does include allergen advisory statement: Made in a facility that processes peanuts, milk, eggs, wheat, soy, tree nuts, fish, shellfish, and sesame products .

Lot/Code Info: Packed on Date: April 5, 2023 Sell Thru Date: April 17, 2023

Quantity Affected: 11 units

Reason for Recall

Undeclared peanut and soy.

Distribution

distributed in WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-09

Company

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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Albertsons Companies LLC has 174 FDA actions in our database, including 174 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 (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Albertsons Companies LLC have FDA actions?

Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0955-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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