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Showing 2841–2860 of 3363 results

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Gelnique Gel (Actavis) – Drug Potency Compromise (2014)

Subpotent Drug: Drug potency was compromised during shipment.

FDAFeb 7, 2014Nationwide• Actavis

Organic Sweet Greens Juice (Evolution Fresh) – Precautionary Recall (2014)

Evolution Fresh is recalling Organic Sweet Green and Ginger Juice out of an abundance of caution.

FDAFeb 7, 2014CA, NV, TX• Evolution Fresh Inc

Vitamin D Milk (Borden Dairy) – Vitamin Overload (2014)

The firm was informed that the product has more than double the labeled amount of Vitamin D. The target minimum level is 400 IU per Qt. The product contains 1006 IU per Qt.

Class IIILow

FDAFeb 6, 2014IN, KY, OH +1 more• Borden Dairy Co Of Cincinnati Llc

Tussin CF Cold Liquid (Aaron Industries) – Precipitate Presence (2014)

Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.

FDAFeb 4, 2014Nationwide• Aaron Industries Inc

Zele Bonboni Jelly Candy (Fast-Pak) – Unauthorized Color (2014)

NYSDAM laboratory analysis report has revealed that Zele Bonboni Jelly Candy contains unallowed green colorant chlorophillyn.

FDAFeb 4, 2014NY• Fast-Pak Trading Inc.

Chicken Demi-Glace Xpress (New Horizon) – Spoiled Chicken Ingredient (2014)

Product was manufactured using chicken that was reported to be spoiled by another government agency.

FDAJan 31, 2014IL, IA, MI• New Horizon Cuisine

DermOtic Ear Drops (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

DermOtic Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Fluocinolone Acetonide Topical Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Derma-Smoothe Scalp Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Fluocinolone Acetonide Ear Drops (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Derma-Smoothe Body Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Fluocinolone Acetonide Body Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Derma-Smoothe Topical Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Derma-Smoothe Scalp Oil (Hill Dermaceuticals) – Low Potency (2014)

Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.

FDAJan 31, 2014Nationwide• Hill Dermaceuticals, Inc.

Triamcinolone Cream (Fougera) – Labeling Error (2014)

Labeling: Label Error on Declared Strength: There is a misprint on the end flap which read 01% rather than 0.1%.

FDAJan 29, 2014Nationwide• Fougera Pharmaceuticals Inc.

Carisoprodol Tablets (Mylan) – Impurity Specification Failure (2014)

Failed Impurity/degradation Specification

FDAJan 28, 2014Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Suprax Cefixime Suspension (Lupin) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.

FDAJan 27, 2014Nationwide• Lupin Pharmaceuticals Inc.

Suprax Cefixime Suspension (Lupin) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.

FDAJan 27, 2014Nationwide• Lupin Pharmaceuticals Inc.

Green Whole Beans (Bonduelle) – Product Filth (2014)

Laceration Risk

Bonduelle North America has recalled bulk totes of Cut and Whole Green Beans due to the presense of filth

FDAJan 24, 2014AR, IA• Bonduelle USA Inc

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