RecallHawk
Class I Recall

Heinen's Fresh Ground Cashew Butter: packaged in plastic circle containers 1lb. Sold individually.

Heinens

Summary

The FDA issued a Class I for Heinen's Fresh Ground Cashew Butter: packaged in plastic circle containers 1lb. by Heinens. Reason: Undeclared Allergens: Possible Peanut Butter and/or Almond Butter mixed into Cashew Butter container..

Details

Source

Food Recall

External ID

F-1403-2023

Action Date

2023-08-23

Status

Terminated

Category

food

Product Description

Heinen's Fresh Ground Cashew Butter: packaged in plastic circle containers 1lb. Sold individually.

Lot/Code Info: Sell By 08/27/2023 Lot No. 235263 Product No. 409530 Manufacturer No. 19583163552

Quantity Affected: 309 containers

Reason for Recall

Undeclared Allergens: Possible Peanut Butter and/or Almond Butter mixed into Cashew Butter container.

Distribution

Retail Locations in OH and IL

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-13

Company

Heinens

Warrensville Heights, OH

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

Heinens has 2 FDA actions in our database, including 2 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 (Heinens) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Heinens have FDA actions?

Heinens has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1403-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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