RecallHawk
Class II Recall

Zesty Sweet Peppers. Shelf stable product in glass container. Net wt. 8 oz (372 g). The label is read in parts: "***Z

Soul Cedar Farm LLC

Summary

The FDA issued a Class II for Zesty Sweet Peppers. Shelf stable product in glass container. Net wt. 8 oz (372 by Soul Cedar Farm LLC. Reason: Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 5.57..

Details

Source

Food Recall

External ID

F-1298-2022

Action Date

2022-06-22

Status

Terminated

Category

food

Product Description

Zesty Sweet Peppers. Shelf stable product in glass container. Net wt. 8 oz (372 g). The label is read in parts: "***Zesty Sweet Peppers *** Ingredients: Sweet Peppers, Balsamic Vinegar (organic wine vinegar, organic concentrated grape must), Olive Oil, Onion, Lemon Juice, Garlic, Rosemary, Thyme *** Batch** Date Processed *** SOUL CEDAR FARM 124 Center Rd. Chimacum, WA 98325 ***".

Lot/Code Info: Process dates: 5/27/2021 (code ZP05211), 9/13/2021 (ZP09212), 10/8/2021 (ZP10213), 2/5/2022 (ZP02221), and 2/14/2022 (ZP02222). Code Interpretation of ZP02221: ZP is the product (Zest Peppers), 02 is the month (February), 22 is the year (2022), and 1 is the batch number (first batch during 2022).

Quantity Affected: 110/8 oz. jars

Reason for Recall

Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 5.57.

Distribution

Distributed in WA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-18

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 175 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 (Soul Cedar Farm LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Soul Cedar Farm LLC have FDA actions?

This is the only FDA action we have on record for Soul Cedar Farm LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1298-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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