FoodOct 7, 2020
EAGLE FAMILY FOODS GROUP 365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz recall — FDA F-1618-2020
Foreign material, pieces of glass may be in the product
Class IIFDA: TerminatedEAGLE FAMILY FOODS GROUP LLC
Latest records
Latest recalls — page 964
The newest recall records with useful source details are listed here.
FoodOct 7, 2020
Spokane Produce Item 70173 Nacho Mini, Refrigerated, net wt recall — FDA F-1582-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 80827 Roasting Vegetables, Refrigerated, net wt recall — FDA F-1609-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 79090 Onion Yellow Sliced, Refrigerated, net wt recall — FDA F-1607-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 83981 Pico De Gallo Salsa Med Saddlin' Up, Refrigerated recall — FDA F-1588-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
EAGLE FAMILY FOODS GROUP Cretors Organic Extra Virgin Olive Oil Popcorn, 4.4 oz recall — FDA F-1621-2020
Foreign material, pieces of glass may be in the product
Class IIFDA: TerminatedEAGLE FAMILY FOODS GROUP LLC
FoodOct 7, 2020
Spokane Produce Item 78750 Onion Red Sliced, Refrigerated, net wt recall — FDA F-1599-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 79000 Onion Yellow Diced, Refrigerated, net wt recall — FDA F-1602-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 80846 Portabella Caps w/ Spinach, Feta & Pico recall — FDA F-1590-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Spokane Produce Item 80823 Fajita Mix, Refrigerated, net wt recall — FDA F-1593-2020
Salmonella Newport. Product contains onion supplied from Thomson International, Inc.
Class IFDA: TerminatedSpokane Produce, Inc.
FoodOct 7, 2020
Shatto Milk Co Brownie, Chocolate Brownie and Vanilla Ice Cream Sammich, Net recall — FDA F-0003-2021
The firm was informed by their supplier than an ingredient in the cookie portion of their ice cream sandwiches contain the undeclared major food allergen soy (soy lecithin)
Class IIFDA: TerminatedShatto Milk Co
FoodOct 7, 2020
EAGLE FAMILY FOODS GROUP Nice! Organic White Cheddar Popcorn, 4.5 oz recall — FDA F-1623-2020
Foreign material, pieces of glass may be in the product
Class IIFDA: TerminatedEAGLE FAMILY FOODS GROUP LLC
FoodOct 7, 2020
EAGLE FAMILY FOODS GROUP 365 Everyday Value Organic Classic Salted Popcorn, 6 oz recall — FDA F-1620-2020
Foreign material, pieces of glass may be in the product
Class IIFDA: TerminatedEAGLE FAMILY FOODS GROUP LLC
FoodOct 7, 2020
EAGLE FAMILY FOODS GROUP 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn, 6 recall — FDA F-1619-2020
Foreign material, pieces of glass may be in the product
Class IIFDA: TerminatedEAGLE FAMILY FOODS GROUP LLC
DrugOct 7, 2020
4e Brands blumen ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT, (ethyl alcohol 70% v/v) recall — FDA D-0031-2021
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Class IFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
Direct Rx Losartan Pot/HCTZ 50/12.5 mg 90 Tabs Packaged and recall — FDA D-0032-2021
CGMP deviation: Trace amounts of impurity detected to be N-Methylnitrosobutyric acid (NMBA) in the API.
Class IIFDA: TerminatedDirect Rx
DrugOct 7, 2020
4e Brands blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural Boost with recall — FDA D-0022-2021
CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Class IIFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
4e Brands blumen Aloe ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT (70% ethyl alcohol v/v) recall — FDA D-0025-2021
CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Class IIFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
4e Brands blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% natural boost with recall — FDA D-0030-2021
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Class IFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
4e Brands blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v) recall — FDA D-0029-2021
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Class IFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
P & L Developments Nicotine Gum, Nicotine Polacrilex Gum USP, 2 mg (nicotine), 110-count recall — FDA D-0004-2021
Labeling: Incorrect or Missing Package Insert: The package insert included in the finished product is for the Canadian market and is not part of the current approved drug labeling.
Class IIIFDA: TerminatedP & L Developments, LLC
DrugOct 7, 2020
4e Brands blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged recall — FDA D-0023-2021
CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Class IIFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
4e Brands ASSURED Instant Hand Sanitizer Aloe & Moisturizers, (70% ethyl alcohol), Packaged recall — FDA D-0027-2021
CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Class IIFDA: Terminated4e Brands North America, LLC
DrugOct 7, 2020
Volu-Sol Handrub Sanitizing Solution recall — FDA D-0033-2021
Marketed Without an Approved NDA/ANDA: product lists methanol as an inactive ingredient on the label.
Class IFDA: TerminatedVolu-Sol, Inc.
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October 2026179 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories