Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1688-2022.
Food and beverage thickener recalled because of possible insanitary conditions during manufacturing
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1688-2022.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Kent Precision Foods Group, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1688-2022.
Kent Precision Foods Group, Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Kent Precision Foods Group, Inc. Recall FAQ
Kent Precision Foods Group, Inc. is the subject of a beverages safety report: Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case. The notice was published on June 9, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 14 units are potentially affected.