RecallHawk
Class II Recall

Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottle UPC 855232007194, 6 bottles per wholesale case

KRAFT HEINZ FOODS COMPANY

Summary

The FDA issued a Class II for Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottle UPC 855232007194, by KRAFT HEINZ FOODS COMPANY. Reason: The product's glass bottle may be prone to breakage.

Details

Source

Food Recall

External ID

F-1482-2024

Action Date

2024-07-24

Status

Terminated

Category

food

Product Description

Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottle UPC 855232007194, 6 bottles per wholesale case

Lot/Code Info: Best When Used By date of 19 Aug 2025 through 21 Aug 2025.

Quantity Affected: 2,061 cases

Reason for Recall

The product's glass bottle may be prone to breakage

Distribution

ME, CA, GA, IN, KY, NC, NV, PA, AZ, TX and online nationally

Type: Voluntary: Firm initiated

Recall Initiated: 2024-04-19

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.

KRAFT HEINZ FOODS COMPANY has 16 FDA actions in our database, including 16 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (KRAFT HEINZ FOODS COMPANY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does KRAFT HEINZ FOODS COMPANY have FDA actions?

KRAFT HEINZ FOODS COMPANY has 16 FDA actions in our database, including 16 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1482-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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