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.
Monthly breakdown
2015 recalls by month
Select a month to review the recall records reported during that period.
December 201593 records · 2 categoriesNovember 2015364 records · 2 categoriesOctober 2015140 records · 2 categoriesSeptember 2015269 records · 2 categoriesAugust 2015193 records · 2 categoriesJuly 2015660 records · 2 categoriesJune 2015111 records · 2 categoriesMay 2015295 records · 2 categoriesApril 2015719 records · 2 categoriesMarch 2015168 records · 2 categoriesFebruary 2015284 records · 2 categoriesJanuary 201543 records · 2 categories
2015 recalls — page 35
Records are ordered by the best available source date.
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.
DrugSep 2, 2015
Liberty Drug & Surgical Papaverine/Phentolamine/PGE-1 Injectable, 30 mg/2 mg/20 mcg/mL, 2.5 recall — FDA D-1384-2015
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
Pharmedium Services HEPARIN Sodium Injection USP 25,000 USP Units added to 250 mL 5% recall — FDA D-1357-2015
Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were subsequently recalled by the manufacturer due…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 2, 2015
Liberty Drug & Surgical Cyanocobalamin 500 mcg/mL Injectable, 1 mL pre-filled syringe recall — FDA D-1380-2015
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
About the 2015 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.