RecallHawk
Class I Recall

4-lb. bags of Kirkland Signature Frozen Organic Strawberries 9 bags per carton - 36 lbs. per carton

California Splendor, Inc.

Summary

The FDA issued a Class I for 4-lb. bags of Kirkland Signature Frozen Organic Strawberries 9 bags per carton - by California Splendor, Inc.. Reason: Product may be contaminated with Hepatitis A.

Details

Source

Food Recall

External ID

F-0700-2023

Action Date

2023-04-19

Status

Terminated

Category

food

Product Description

4-lb. bags of Kirkland Signature Frozen Organic Strawberries 9 bags per carton - 36 lbs. per carton

Lot/Code Info: Lot numbers/Best if Used By: 140962-08 4/6/2024, 142162-20 8/4/2024, 142202-21 8/8/2024, 142212-22 8/9/2024, 142222-23 8/10/2024, 142232-24 8/11/2024, 142782-53 10/5/2024, 142792-54 10/6/2024, 142842-55 10/11/2024, 142852-56 10/12/2024, 142862-57 10/13/2024, 142902-58 10/17/2024, 142912-59 10/18/2024, 143482-91

Quantity Affected: 418,604 lbs.

Reason for Recall

Product may be contaminated with Hepatitis A

Distribution

Product was distributed to Oregon and California

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-15

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

California Splendor, Inc. has 3 FDA actions in our database, including 3 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 (California Splendor, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does California Splendor, Inc. have FDA actions?

California Splendor, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0700-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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