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UNFI General Corporate

UNFI General Corporate Recalls

All product recalls associated with UNFI General Corporate.

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Recall Summary

Total Recalls

1000

Past Year

123

Class I (Serious)

69

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1081–1100 of 2383 recalls

Unbleached All-Purpose Flour (Essential Everyday) – Salmonella risk (2019)

Product was found positive for Salmonella

Class IIModerate

FDADec 13, 2019Nationwide• UNFI General Corporate

Honey Bear Platter (Mrs. Condies) – Undeclared Milk (2019)

Undeclared Milk

Ranch Dressing dip contains undeclared milk as an ingredient.

FDADec 3, 2019CO• Mrs. Condies Salad Company, Incorporated

HeartMate 3 Mobile Power Unit (Thoratec) – Static Electricity Risk (2019)

Excessive static electricity can potentially cause unrecoverable power loss and damage to the mobile power unit that can be used to power the left ventricular assist system, which could lead to no or reduced blood flow from the left ventricular assist system.

1...53 545556 57...120

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FDADec 2, 2019Nationwide• Thoratec Corp.

Soft Tissue Retractor (AAP) – Removal Risk (2019)

The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris can develop and remain in vivo.

FDANov 28, 2019Nationwide• AAP Implantate Ag Lorenzweg 5 Berlin Germany

Petroleum Jelly (OraLabs) – Contaminant Cross-Contamination (2019)

Undeclared Allergen

Cross contamination with other products: undeclared contaminants of phenol and camphor in petroleum jelly tubes.

Class IIModerate

FDANov 25, 2019Nationwide• OraLabs, Incorporated

Gore DrySeal Flex Introducer Sheath, Catalog #DSF1433, 33... (W. L. Gore & Associates Inc.) – mislabeling (2019)

The devices were mislabeled with the incorrect product size resulting in 16Fr devices being labeled as 14Fr devices.

FDANov 18, 2019Nationwide• W. L. Gore & Associates Inc.

Formoterol Budesonide Inhalation (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium Inhalation (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium Triamcinolone (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Budesonide Inhaler (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Budesonide Inhalation Vial (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Great Value Glazed Donuts (US Bakery) – Packaging Glue Issue (2019)

Great Value Old Fashioned Glazed Donuts are recalled because packaging glue inside the box was found.

FDANov 8, 2019AR, GA, IN +4 more• United States Bakery Corp

Pip Pop Movie Theater Popcorn (Water Gardens) – Foreign Material (2019)

Foreign material determined to be part of packaging was found in 24 oz. bags of Pip Pop Movie Theater Popcorn produced on multiple dates.

Class IIModerate

FDANov 7, 2019CO, ID, IN +4 more• Water Gardens Confections LLC

Ranitidine Capsules 150mg (Golden State Medical) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDANov 6, 2019AZ, IA, MA +1 more• Golden State Medical Supply Inc.

Ranitidine Capsules 300mg (Golden State Medical) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDANov 6, 2019AZ, IA, MA +1 more• Golden State Medical Supply Inc.

Potassium Phosphate (Avantor) – Exceeded Iron Specs (2019)

Failed Stability Specifications: Product exceeds compendia and firm's specifications for iron content.

Class IIModerate

FDAOct 30, 2019Nationwide• Avantor Performance Materials Inc

Taspen's Respiratory Tea (Green Water) – Unsafe Ingredient (2019)

The products contain Coltsfoot, which is not to be used internally.

Class IIModerate

FDAOct 24, 2019Nationwide• Green Water, LLC

Taspen's Breathe Easy Tincture (Green Water) – Unsafe Ingredient (2019)

The products contain Coltsfoot, which is not to be used internally.

Class IIModerate

FDAOct 24, 2019Nationwide• Green Water, LLC

Dragonfly Breathe Deep Supplement (Green Water) – Unsafe Ingredient (2019)

The products contain Coltsfoot, which is not to be used internally.

Class IIModerate

FDAOct 24, 2019Nationwide• Green Water, LLC