Natural Pak brand Bacon Glaze is packaged in
Reason Package actually contains "Coffee Chili Rub" resulting in sea salt, ancho chile, espresso beans, mustard, coriander, ginger, oregano, chipotle chile being undeclared on the label
Natural Pak brand Coffee Chili Rub is packaged in recall
Recalled by Victoria Gourmet, Inc. · Woburn, MA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Package contains "Bacon Glaze" resulting in: demerara sugar, honey granules, maple sugar, cinnamon, all spice, clove, parsley being undeclared on the label
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
Natural Pak brand Coffee Chili Rub is packaged in 22oz (624g), white, cylindrical, plastic containers; Ingredients: Sea salt, ancho chile, brown sugar, espresso beans, hot smoked paprika, mustard, black pepper, coriander, ginger, oregano, chipotle chile, paprika. Contains: mustard
Quantity: 36 units
Food: Juice & beverages
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.
BEST IF USED BY 12/2025 and Lot #L2332402; 4C42/4L33 UPC: 666227804069
Where it was sold
Ohio
FDA's distribution note: OH
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
- Victoria Gourmet, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 22, 2023
- In FDA report of
- Apr 26, 2023
- Terminated
- Jul 27, 2023
- FDA recall number
- F-0747-2023 · event 91945
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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