796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part #020001965. Ingredients: Sugar, Salt,
Summary
The FDA issued a Class III for 796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part # by PS Seasoning & Spices, Inc.. Reason: Undeclared wheat..
Details
Source
Food Recall
External ID
F-0871-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part #020001965. Ingredients: Sugar, Salt, Spice, Brown Sugar, Dried Honey, Hot Sauce Powder (aged Cayenne Red Peppers, Vinegar, Salt, Garlic), Garlic Powder, Sodium Diacetate, Sodium Erythorbate (0.238%), Natural Flavors.
Lot/Code Info: Lot numbers: 2021-48540, and 2022-51895.
Quantity Affected: 398 units
Reason for Recall
Undeclared wheat.
Distribution
AR, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MD, MI, MN, MO, MT, ND, NE, NH, NY, OH, OK, PA, SD, WA, WI, WY, and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-18
Company
Iron Ridge, WI
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
PS Seasoning & Spices, Inc. has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (PS Seasoning & Spices, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does PS Seasoning & Spices, Inc. have FDA actions?
PS Seasoning & Spices, Inc. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0871-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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