Recall record at a glance
| Official record | F-1530-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | The C.F. Sauer Company |
| Report date | Jun 13, 2018 |
| Recall initiation date | May 4, 2018 |
| Quantity | 53 Cases |
| Location | Richmond, VA, United States |
Official 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
Why the product was recalled
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.
Distribution information
Product has been distributed to: Georgia, Illinois, North Carolina, Pennsylvania, Rhode Island, South Carolina, Virginia, and Wisconsin.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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