RecallHawk
Class III Recall

Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL OZ (148 mL) UPC 75 03016 55511 1 packaged in a PET bottle, 12 bo

TIPPCON LLC

Summary

The FDA issued a Class III for Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL OZ (148 mL) UPC 75 03016 by TIPPCON LLC. Reason: Mold growth on the outside of the bottle.

Details

Source

Food Recall

External ID

F-0710-2023

Action Date

2023-04-19

Status

Terminated

Category

food

Product Description

Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL OZ (148 mL) UPC 75 03016 55511 1 packaged in a PET bottle, 12 bottles per case

Lot/Code Info: Codes: 1.323122, 2.323122, 3.323222, 4.323222, 5.323422, 6.323422, 7.323422

Quantity Affected: 8,230 cases (total)

Reason for Recall

Mold growth on the outside of the bottle

Distribution

Nationwide (USA).

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-13

Company

TIPPCON LLC

El Paso, TX

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

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

How often does TIPPCON LLC have FDA actions?

TIPPCON LLC 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-0710-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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