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Soul Cedar Farm LLC Recall: Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 5.57.

United States

TerminatedClass II

Company
Soul Cedar Farm LLC
Product
Zesty Sweet Peppers. Shelf stable product in glass container…
Recall date
April 18, 2022
Terminated
June 10, 2022
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 ***". Not published in this source record 110/8 oz. jars 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).

Distribution

  • Distributed in WA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1298-2022
Event ID
90206
Status
Terminated
Classification
Class II
Company
Soul Cedar Farm LLC
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 ***".
Quantity
110/8 oz. jars
Reason
Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 5.57.
Recall initiation date
April 18, 2022
Report date
June 22, 2022
Classification date
Not published in this source record
Termination date
June 10, 2022
Distribution pattern
Distributed in WA
UPC, lot, and code information
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).
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Soul Cedar Farm LLC

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Washington 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.