Class IIITerminated in FDA datasetRecall initiated Mar 22, 2023

Natural Pak brand Coffee Chili Rub is packaged in 22oz (624g), white, cylindrical, plastic…

Recalling firm: Victoria Gourmet, Inc.

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 27, 2023.

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ProductNatural 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
Package size22oz
UPC666227804069

FDA code information

BEST IF USED BY 12/2025 and Lot #L2332402; 4C42/4L33 UPC: 666227804069

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC666227804069BEST IF USED BY 12/2025 and Lot #L2332402; 4C42/4L33 UPC: 666227804069
lot4C42/4L33BEST IF USED BY 12/2025 and Lot #L2332402; 4C42/4L33 UPC: 666227804069
lotL2332402BEST IF USED BY 12/2025 and Lot #L2332402; 4C42/4L33 UPC: 666227804069

Original FDA recall reason

Package contains "Bacon Glaze" resulting in: demerara sugar, honey granules, maple sugar, cinnamon, all spice, clove, parsley being undeclared on the label

Recall details

Recall number
F-0747-2023
Event ID
91945
FDA status
Terminated
Initiated
Mar 22, 2023
Reported
Apr 26, 2023
Classified
Apr 20, 2023
Terminated
Jul 27, 2023
Quantity
36 units
Location
Woburn, MA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

OH

FDA source record · F-0747-2023

Data updated September 16, 2026. View official FDA data ↗

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