DrugApr 9, 2014
Tivicay (dolutegravir) Tablets 50 mg, 30 Tablet Bottles recall — FDA D-1185-2014
Cross Contamination with Other Products: Product contains Promacta (eltrombopag).
Class IIIFDA: TerminatedViiv Healthcare Company
Monthly breakdown
2014 recalls by month
Select a month to review the recall records reported during that period.
December 2014206 records · 2 categoriesNovember 2014617 records · 2 categoriesOctober 2014159 records · 2 categoriesSeptember 2014101 records · 2 categoriesAugust 2014118 records · 2 categoriesJuly 2014224 records · 3 categoriesJune 201483 records · 2 categoriesMay 2014120 records · 2 categoriesApril 2014219 records · 2 categoriesMarch 2014137 records · 2 categoriesFebruary 201484 records · 2 categories
2014 recalls — page 77
Records are ordered by the best available source date.
DrugApr 9, 2014
Teva Pharmaceuticals USA Duloxetine Delayed-Release Capsules, USP, 60 mg recall — FDA D-1184-2014
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend…
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugApr 9, 2014
Lupin Pharmaceuticals Suprax, Cefixime for Oral Suspension USP 500 mg/5 ml, 10mL recall — FDA D-1186-2014
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugApr 9, 2014
Lupin Pharmaceuticals Suprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL recall — FDA D-1187-2014
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
FoodApr 2, 2014
Plum Stage 2 World Baby recall — FDA F-1688-2014
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two product dates may cause plastic fragments to break loose and cause a potential…
Class IIFDA: TerminatedPlum Inc.
FoodApr 2, 2014
Crown Food Distributors Golden Natural Fruit Island Net Wt recall — FDA F-1701-2014
NYSDAM analysis has revealed the presence of undeclared sulfites and undeclared FD&C Yellow #6 in Golden Natural Brand "Fruit Island".
Class IFDA: TerminatedCrown Food Distributors Inc.
FoodApr 2, 2014
Wolfgang B. Gourmet Foods FAIRWAY brand CONDIMENT GRILLING SAUCE, NET WT 12 oz recall — FDA F-1684-2014
The Grilling Sauce contains undeclared fish (anchovies), a a sub-ingredient in the Worcestershire Sauce ingredient used in making the product.
Class IIFDA: TerminatedWolfgang B. Gourmet Foods, Inc.
FoodApr 2, 2014
HP Hood my essentials brand sour cream, NET WT recall — FDA F-1690-2014
HP Hood LLC received one complaint of a foreign object in sour cream product with APR 05 14 code. The object was subsequently identified to be part of a metal bolt from a filling machine.
Class IIFDA: TerminatedHP Hood LLC
FoodApr 2, 2014
Plum Stage 2 World Baby Thailand recall — FDA F-1687-2014
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two production dates may cause plastic fragments to break loose and cause a potential…
Class IIFDA: TerminatedPlum Inc.
FoodApr 2, 2014
New Horizon Cuisine packaged in 16-oz recall — FDA F-1697-2014
Product was manufactured using chicken that was reported to be spoiled by another government agency.
Class IIIFDA: TerminatedNew Horizon Cuisine
FoodApr 2, 2014
Dole Fresh Vegetables Italian blend Salad recall — FDA F-1702-2014
Canadian Food Inspection Agency tested a random sample of bagged Italian Blend which tested positive for Listeria Monocytogenes.
Class IFDA: TerminatedDole Fresh Vegetables Inc.
FoodApr 2, 2014
Mars Food US UNCLE BEN's recall — FDA F-1686-2014
Voluntary recall was initiated after identifying a number of packages with punctures on the back of the package that led to spoilage (off odors and appearance).
Class IIFDA: TerminatedMars Food US
FoodApr 2, 2014
Nutra Balance Products Thickened Water Nectar Thick 32 oz recall — FDA F-1700
NUTRA Balance Thickened Water Nectar Thick was found by the FDA to contain mold. In addition, Thickened Water Pudding thick was sampled by Nutra Balance Products and it subsequently tested…
Class IIFDA: TerminatedNutra Balance Products
FoodApr 2, 2014
Chicken Soup For The Soul Food 32 oz recall — FDA F-1683-2014
Product contains undeclared wheat
Class IIFDA: TerminatedChicken Soup For The Soul Food
DrugApr 2, 2014
DERMA-SMOOTHE/FS ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% recall — FDA D-1177-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil recall — FDA D-1180-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
DERMA-SMOOTHE/FS ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical recall — FDA D-1176-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops, 20 mL bottle recall — FDA D-1173-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 recall — FDA D-1174-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
DERMOTIC ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops), 20 ml recall — FDA D-1178-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS, 20 ml recall — FDA D-1181-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 recall — FDA D-1175-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
DrugApr 2, 2014
Hill Dermaceuticals SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil recall — FDA D-1179-2014
Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Class IIIFDA: TerminatedHill Dermaceuticals, Inc.
FoodMar 26, 2014
CSM Bakery Products 10" Chocolate Supreme Cake Layers, NET WT recall — FDA F-1681-2014
Foreign Material - specifically the product has the potential to contain pieces of a red plastic scoop.
Class IIFDA: TerminatedCSM Bakery Products North America
About the 2014 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.