The C.F. Sauer Company Recall: The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.

🇺🇸 United States

1. May 4, 2018 - Recall initiated
2. June 13, 2018 - Reported by source
3. December 13, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1530-2018

Event ID

80075

Status

Terminated

Classification

Class II

Company

The C.F. Sauer Company

Product description

Sauer - Red Pepper Seasoning (21 oz.) Net Weight: 21 oz., Number of Units per Package: 6 Package Type: clear, 32 fl. oz. polyethylene terephthalate bottle , Units per case: 6

Quantity

53 Cases

Reason

The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.

Recall initiation date

May 4, 2018

Report date

June 13, 2018

Classification date

Not published in this source record

Termination date

December 13, 2018

Distribution pattern

Product has been distributed to: Georgia, Illinois, North Carolina, Pennsylvania, Rhode Island, South Carolina, Virginia, and Wisconsin.

UPC, lot, and code information

Lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R.

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 80075 with 4 other product entries in Public Health Trace.

Responsible company: The C.F. Sauer Company

Other recalls from The C.F. Sauer Company

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: July 18, 2026 ET

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.

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