FoodSep 2, 2015
Fresh Unlimited Kale Chicken Caesar Pasta Salad, 3.87# recall — FDA F-3052-2015
The firm failed to declare the allergen eggs on their labels.
Class IFDA: TerminatedFresh Unlimited Inc.
September 2015 recalls — page 10
These records include useful source details for the selected month.
FoodSep 2, 2015
It Takes A Village Foods Kale Crisps Lemon Parmesan sold under brand Veggie Evolution recall — FDA F-3049-2015
Kale Crisps Lemon Parmesan is recalled because label declared Parmesan cheese but milk is not declared.
Class IIFDA: TerminatedIt Takes A Village Foods, LLC
FoodSep 2, 2015
The Kroger Co Kroger Ground Cinnamon UPC 11110 70034 NEW WT recall — FDA F-3043-2015
The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is…
Class IFDA: TerminatedThe Kroger Co
FoodSep 2, 2015
Fresh Unlimited Caesar Salad, #5.56 recall — FDA F-3051-2015
The firm failed to declare the allergen eggs on their labels.
Class IFDA: TerminatedFresh Unlimited Inc.
DrugSep 2, 2015
GlaxoSmithKline, LLC Bactroban (mupirocin calcium) Nasal Ointment, 2% 1g tube recall — FDA D-1359-2015
Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.
Class IIFDA: TerminatedGlaxoSmithKline, LLC.
DrugSep 2, 2015
Liberty Drug & Surgical Papaverine/Phentolamine/Atropine/PGE-1 Injectable, 9 mg/1 mg/0.1 recall — FDA D-1383-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Liberty Drug & Surgical Doxycycline/0.9% NaCl 300 mg/500 mL IV, 500 mL bag recall — FDA D-1401-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Liberty Drug & Surgical Dexamethasone 24 mg/mL Injectable, 1 mL vial recall — FDA D-1395-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Topicort (desoximetasone) Topical Spray, 0.25%, 100 mL Bottles recall — FDA D-1370-2015
Failed Impurities/Degradation Specifications: Out of specification results for impurities testing was obtained at the 6 and 9 month time points.
Class IIIFDA: TerminatedTaro Pharmaceuticals, Inc.
DrugSep 2, 2015
Liberty Drug & Surgical Tobramycin 14 mg/mL Ophthalmic Solution, 15 mL bottle recall — FDA D-1389-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Hydrochlorothiazide Tablet USP 25 mg,1000- count bottle recall — FDA D-1352-2015
Presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothiazide 25 mg tablets.
Class IIFDA: TerminatedUnichem Pharmaceuticals Usa Inc.
DrugSep 2, 2015
Liberty Drug & Surgical Doxycycline/0.9 % NaCl 100 mg/100 mL IV, 100 mL bag recall — FDA D-1390-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
GlaxoSmithKline, LLC Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube recall — FDA D-1362-2015
Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.
Class IIFDA: TerminatedGlaxoSmithKline, LLC.
DrugSep 2, 2015
Amlodipine besylate and Atorvastatin calcium Tablets,10 mg/40 mg recall — FDA D-1378-2015
Subpotent Drug: Subpotent atorvastatin.
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugSep 2, 2015
Liberty Drug & Surgical Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial recall — FDA D-1382-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Teva Pharmaceuticals USA ADRUCIL recall — FDA D-1351-2015
Presence of Particulate Matter: silcone rubber and fluorouracil crystals found floating in solution
Class IFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 2, 2015
Mucinex Fast Max DM Max, Maximum Strength, Dextromethorphan HBr Cough Suppressant, 6 fl oz recall — FDA D-1369-2015
Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing…
Class IIFDA: TerminatedReckitt Benckiser LLC
DrugSep 2, 2015
Reckitt Benckiser Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu recall — FDA D-1366-2015
Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing…
Class IFDA: TerminatedReckitt Benckiser LLC
DrugSep 2, 2015
Liberty Drug & Surgical Glycerin (v/v) 72% Injection, 25 mL vial recall — FDA D-1397-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Reckitt Benckiser Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu recall — FDA D-1368-2015
Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing…
Class IFDA: TerminatedReckitt Benckiser LLC
DrugSep 2, 2015
Liberty Drug & Surgical Papaverine/Phentolamine/PGE-1 Injectable, 20.8 mg/1.4 mg/14 mcg/mL recall — FDA D-1386-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Liberty Drug & Surgical Morphine/0.9 % NaCl 1 mg/mL IV, 250 mL bag recall — FDA D-1396-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Liberty Drug & Surgical Papaverine/Phentolamine/PGE-1 Injectable, 10 mg/0.6 mg/10 mcg/mL recall — FDA D-1385-2015
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Class IIFDA: TerminatedLiberty Drug & Surgical
DrugSep 2, 2015
Amlodipine besylate and Atorvastatin calcium Tablets, 5 mg/20 mg recall — FDA D-1376-2015
Subpotent Drug: Subpotent atorvastatin.
Class IIIFDA: TerminatedDr. Reddy's Laboratories, 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.