Woburn, MA, United States
Victoria Gourmet, Inc. recalls
3 recalls recorded since 2018, most recently on 22 March 2023. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)0
Terminated or completed3
Class I (FDA)0
Terminated Class III Food
- Recall started
- 22 March 2023
- Terminated
- 27 July 2023
- 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
- Distribution
- OH
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- F-0746-2023, F-0747-2023
- Natural Pak brand Bacon Glaze is packaged in 22.9oz (649g), white, cylindrical, plastic containers; Ingredients: Demerara sugar, honey granules, brown sugar, maple sugar, paprika, spices (black pepper, cinnamon, allspice
- 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
Terminated Class II Food
- Recall started
- 17 November 2020
- Terminated
- 14 December 2020
- Reason
- Product contains undeclared sesame.
- Distribution
- Canada only.
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0162-2021
- Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in a glass jar. Canadian product only.
Terminated Class III Food
- Recall started
- 21 September 2018
- Terminated
- 24 October 2018
- Reason
- Product labeling is incorrect.
- Distribution
- IN, WA, AK, CA, PA, HI, NY, MO, CA, TX, WI, CT, DE, NC, MI, FL, SC, MA
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- F-0059-2019, F-0060-2019
- Victoria Taylor's Seasonings - Blackening Rub, 6.4 oz., UPC: 666227015274, packaged in a glass jar with a lid
- Victoria Taylor's Seasonings - New Orleans - 5.0 oz. UPC: 666227015090, packaged in a glass jar with lid
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.