RecallHawk
Class III Recall

Banana Pepper Rings 16 FL OZ (1PT) 473ml UPC:4056489223863. Packaged in a glass jar with metal lid.

Lidl US TRADING

Summary

The FDA issued a Class III for Banana Pepper Rings 16 FL OZ (1PT) 473ml UPC:4056489223863. Packaged in a glass by Lidl US TRADING. Reason: Container integrity issued (punctured lid).

Details

Source

Food Recall

External ID

F-1063-2024

Action Date

2024-03-20

Status

Terminated

Category

food

Product Description

Banana Pepper Rings 16 FL OZ (1PT) 473ml UPC:4056489223863. Packaged in a glass jar with metal lid.

Lot/Code Info: Best before May/28/2026 L789/23 Best before Jul/28/2026 L1051

Quantity Affected: 23,904 jars

Reason for Recall

Container integrity issued (punctured lid)

Distribution

Distributed to distribution centers and retails stores in MD, NC, VA, GA, SC, PA, NJ, NY and Washington D.C.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-25

Company

Lidl US TRADING

Arlington, VA

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lidl US TRADING has 15 FDA actions in our database, including 15 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lidl US TRADING have FDA actions?

Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1063-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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