RecallHawk
Class I Recall

Produce Packaging Inc. brand Spicy Southwest Grain Bowl in a 11.75oz plastic bowl with a plastic lid. One bowl per case.

Produce Packaging Inc

Summary

The FDA issued a Class I for Produce Packaging Inc. brand Spicy Southwest Grain Bowl in a 11.75oz plastic bow by Produce Packaging Inc. Reason: Undeclared wheat on product label..

Details

Source

Food Recall

External ID

F-1015-2022

Action Date

2022-05-04

Status

Terminated

Category

food

Product Description

Produce Packaging Inc. brand Spicy Southwest Grain Bowl in a 11.75oz plastic bowl with a plastic lid. One bowl per case.

Lot/Code Info: Lots: X0736829 and X0740519 Product Number: PP#51648 Best Buy Dates: 04/12/22-04/20/22

Quantity Affected: 21 cases

Reason for Recall

Undeclared wheat on product label.

Distribution

Products were distributed to IL and OH.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-14

Company

Produce Packaging Inc

Willoughby Hills, 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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Produce Packaging 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 (Produce Packaging Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Produce Packaging Inc have FDA actions?

Produce Packaging 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-1015-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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