FoodJul 22, 2015
Sysco International Whole Segments Mandarin Oranges In Light recall — FDA F-2844-2015
Product tested positive for Carbendazim.
Class IIIFDA: TerminatedSysco Corporation
July 2015 recalls — page 3
These records include useful source details for the selected month.
FoodJul 22, 2015
Ungar's Food Products Dr recall — FDA F-2852-2015
Dr. Praeger's Gluten Free California Burgers contain undeclared soy.
Class IFDA: TerminatedUngar's Food Products, Inc.
FoodJul 22, 2015
Dr. Pepper Snapple Group Diet Bubba Cola, 20 FL recall — FDA F-2848-2015
The firm was notified by one of it's retail stores that the ingredient statement does not declare citric acid, potassium benzoate, aspartame, and acesulfame potassium. The product contains…
Class IIIFDA: TerminatedDr. Pepper Snapple Group Inc.
FoodJul 22, 2015
Tortilleria Provincia Net Wt recall — FDA F-2851-2015
The firm used the same label clear plastic bags with Nutrition Facts and Ingredients listed for all three type corn tortillas (Yellow, White, and Blue); the color Yellow # 2 was written in…
Class IIFDA: TerminatedTortilleria Provincia
FoodJul 22, 2015
Vitamin Cottage Natural Food Markets Natural Grocers Caribbean Fruit & Nut Mix, Net Wt recall — FDA F-2854-2015
Vitamin Cottage Natural Food Markets, Inc is recalling one lot of Natural Grocers brand Caribbean Nut & Fruit Mix as the product contains macadamia nuts that have the potential to be…
Class IFDA: TerminatedVitamin Cottage Natural Food Markets, Inc.
FoodJul 22, 2015
Kraft Foods CapriSun Pack, with a multi colored plastic wrap with white recall — FDA F-2853-2015
Possible brass fragments in Capri Sun Fruit Punch Flavored Juice Drink Blend.
Class IIFDA: TerminatedKraft Foods North America
DrugJul 22, 2015
Kremers Urban Pharmaceuticals Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2), For recall — FDA D-1236-2015
Failed Impurities/Degradation Specifications: failed specification for unknown impurity at the 24 month stability testing.
Class IIFDA: TerminatedKremers Urban Pharmaceuticals, Inc.
DrugJul 22, 2015
KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M recall — FDA D-1242-2015
Crystallization; identified as calcium salt of Ketorolac
Class IIFDA: OngoingHospira Inc.
DrugJul 22, 2015
Geritrex Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube recall — FDA D-1238-2015
CGMP Deviation: Poor container closure of the bulk storage container
Class IIIFDA: TerminatedGeritrex Corp
DrugJul 22, 2015
KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M recall — FDA D-1241-2015
Crystallization; identified as calcium salt of Ketorolac
Class IIFDA: OngoingHospira Inc.
DrugJul 22, 2015
Rifampin for Injection, USP 600mg/vial in a 20mL vial recall — FDA D-1234-2015
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation
Class IIFDA: TerminatedFresenius Kabi USA, LLC
DrugJul 22, 2015
Kremers Urban Pharmaceuticals Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2), For recall — FDA D-1237-2015
Failed Impurities/Degradation Specifications: Two lots failed specification for unknown impurity at the 24 month stability testing.
Class IIFDA: TerminatedKremers Urban Pharmaceuticals, Inc.
DrugJul 22, 2015
American Health Packaging Desmopressin Acetate Tablets, 0.1 mg Tablets recall — FDA D-1235-2015
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Class IIIFDA: TerminatedAmerican Health Packaging
FoodJul 15, 2015
Paradigm Foodworks Salsa, All Natural Mild, Hazelwood's brand, Net Wt recall — FDA F-2834-2015
Salsa, All Natural Mild, Hazelwood's brand, containing ground cumin and mild chili powder ingredients, is recalled due to potential for contamination with peanut protein.
Class IIFDA: TerminatedParadigm Foodworks, Inc.
FoodJul 15, 2015
Kerry Foods Kraft French Vanilla, Creamer, Non-Dairy Creamer, Net recall — FDA F-2788-2015
Kerry, Inc. is voluntarily recalling all Nondairy Creamer produced between May 12, 2015 and May 28, 2015 due to the potential for a few packages to contain small pieces of metal from a…
Class IIFDA: TerminatedKerry Foods
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2813-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2804-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2803-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
FoodJul 15, 2015
Paradigm Foodworks Cilantro Salsa, All Natural Medium, Hazelwood's brand, Net Wt recall — FDA F-2823-2015
Cilantro Salsa, All Natural Medium, Hazelwood's brand, containing ground cumin ingredient, is recalled due to potential for contamination with peanut protein.
Class IIFDA: TerminatedParadigm Foodworks, Inc.
FoodJul 15, 2015
Paradigm Foodworks Medium Salsa, D.A.M brand, Net Wt recall — FDA F-2831-2015
Medium Salsa, D.A.M brand, containing ground cumin ingredient, is recalled due to potential for contamination with peanut protein.
Class IIFDA: TerminatedParadigm Foodworks, Inc.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2799-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
FoodJul 15, 2015
New Punjab Sweets New Punjab Ladoo is a ball-shaped Indian snack coated with recall — FDA F-2425-2015
This voluntary recall is being initiated because the following Indian snack lacks an ingredient label. Product may contain undeclared nuts (almonds, pistachios), undeclared colors (Yellow…
Class IIFDA: TerminatedNew Punjab Sweets Inc.
FoodJul 15, 2015
Paradigm Foodworks Hot Pineapple Smash Salsa, Soog Head brand, Net Wt recall — FDA F-2825-2015
Hot Pineapple Smash Salsa, Soog Head brand, containing mild chili powder ingredient, is recalled due to potential for contamination with peanut protein.
Class IIFDA: TerminatedParadigm Foodworks, Inc.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2814-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.