Food Recall Check
Class III · Low risk Terminated Initiated Mar 29, 2024 (3 years ago)

Windsor Black Peppercorns recall

Recalled by Morton Salt INC · Chicago, IL, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Label mix-up product is labeled as black peppercorn but is actually Pink Himalayan salt

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Windsor Black Peppercorns, 34g grinder, UPC 0 66010 08200 9, 6 units per wholesale case

Quantity: 1423 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

lot code, ZX23060001

Where it was sold

FDA's distribution note: Canada

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Morton Salt INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 29, 2024
In FDA report of
Apr 24, 2024
Terminated
Jan 31, 2025
FDA recall number
F-1149-2024 · event 94344
Official record
FDA enforcement report search

Other recalls by Morton Salt INC

Class III · Low risk Terminated Labeling

Morton Iodized Salt

Reason Product labeled to contain iodized salt actually contain salt not fortified with iodine.

Morton Salt INC CA, CO F-0334-2022
Class III · Low risk Terminated Labeling

Morton Salt This Salt Does Not Supply Iodide

Reason Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.

Morton Salt Inc. NC F-0682-2020