RecallHawk
Class II Recall

Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. This product contains peppers in 8 differen

Something South African LLC

Summary

The FDA issued a Class II for Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. Thi by Something South African LLC. Reason: Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A..

Details

Source

Food Recall

External ID

F-0263-2023

Action Date

2023-01-25

Status

Terminated

Category

food

Product Description

Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. This product contains peppers in 8 different glass tube and packaged in a printed paperboard sleeve and are visible through a window in the sleeve. Net wt. is 4.87oz/138g. The UPC is 6 009686 793712. Packed in South Africa. US Importer: Something South African, LLC Seattle WA 98199, Email: info@somethingsouthafrican.net.

Lot/Code Info: BBE: JUN/2024. Batch: 494951 -T

Quantity Affected: 4200 units

Reason for Recall

Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.

Distribution

nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-12

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

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 (Something South African LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Something South African LLC have FDA actions?

This is the only FDA action we have on record for Something South African LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0263-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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