FoodApr 30, 2014
Lisy Sweet Basil Albahaca Net WT/Cont recall — FDA F-1881-2014
FDA sample collected was found to be positive for salmonella spp.
Class IFDA: TerminatedLisy Corp.
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 69
Records are ordered by the best available source date.
FoodApr 30, 2014
CJ Bakery Cinnamon Cookie Manjoo, 200g Net Weight recall — FDA F-1875-2014
CJ Foodville USA, Inc. is recalling its chocolate madeline, madeline, and cinnamon manjoo due to undeclared wheat.
Class IIFDA: TerminatedCJ Bakery, Inc.
FoodApr 30, 2014
CJ Bakery Madeline, 80g Net Weight recall — FDA F-1876-2014
CJ Foodville USA, Inc. is recalling its chocolate madeline, madeline, and cinnamon manjoo due to undeclared wheat.
Class IIFDA: TerminatedCJ Bakery, Inc.
FoodApr 30, 2014
Frontier Natural Products Co-op Whole Black Peppercorns, Certified Organic, Piper nigrum recall — FDA F-1880-2014
Testing of organic whole black peppercorns revealed the presence of Salmonella
Class IFDA: TerminatedFrontier Natural Products Co-op
FoodApr 30, 2014
CJ Bakery Chocolate Madeline, 80g Net Weight recall — FDA F-1877-2014
CJ Foodville USA, Inc. is recalling its chocolate madeline, madeline, and cinnamon manjoo due to undeclared wheat.
Class IIFDA: TerminatedCJ Bakery, Inc.
FoodApr 30, 2014
American Pop Corn Co Jolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton recall — FDA F-1884-2014
The product has the potential to be contaminated with stainless steel metal fragments.
Class IIFDA: TerminatedAmerican Pop Corn Co
DrugApr 30, 2014
GlaxoSmithKline Consumer Healthcare Nicotine polacrilex lozenge, 4 mg, Cherry Flavor, 72 recall — FDA D-1239-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
GlaxoSmithKline Consumer Healthcare Nicotine polacrilex lozenge, 2 mg, Mint Flavor, 81 count recall — FDA D-1242-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
GlaxoSmithKline Consumer Healthcare Nicotine polacrilex lozenge, 4 mg, Mint Flavor, 81 recall — FDA D-1243-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
VPRIV recall — FDA D-1251-2014
Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.
Class IFDA: TerminatedShire Human Genetic Therapies, Inc.
DrugApr 30, 2014
Upsher Smith Laboratories Oxandrolone Tablets, USP, 10 mg recall — FDA D-1255-2014
Labeling: Missing Label; Three cases of product (total of 36 bottles) were packaged without the primary label on the bottle. The cases were, however, packaged in the correct finished…
Class IIIFDA: TerminatedUpsher Smith Laboratories, Inc.
DrugApr 30, 2014
Nicorette (nicotine polacrilex) Lozenges Mini, 2 mg, Original Flavor, 20 Lozenge, 27 recall — FDA D-1245-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
P&L Developments Day Time Cold & Flu, Multi-Symptom, Non-Drowsy, Acetaminophen recall — FDA D-1254-2014
Subpotent Drug: Phenylephrine component is subpotent.
Class IIIFDA: TerminatedP&L Developments, LLC
DrugApr 30, 2014
Pfizer Tikosyn (dofetilide) 500 mcg (0.5mg) capsules, 60-count bottle recall — FDA D-1253-2014
Presence of Foriegn Tablets/Capsules: A single Tikosyn (dofetilide) 250 mcg capsule was discovered in one bottle of Tikosyn (dofetilide) 500 mcg (0.5 mg).
Class IIFDA: TerminatedPfizer Inc.
DrugApr 30, 2014
NICORETTE Nicotine polacrilex lozenge, 4 mg, Original Flavor, 72 count cartons, 81 count recall — FDA D-1240-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
GlaxoSmithKline Consumer Healthcare Nicotine polacrilex lozenge, 2 mg, Cherry Flavor, 72 recall — FDA D-1238-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
Nicorette (nicotine polacrilex) Lozenges Mini, 4 mg, Original Flavor, 20 Lozenge and 81 recall — FDA D-1246-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
NICORETTE Nicotine polacrilex lozenge, 2 mg, Original Flavor, 72 count cartons, 81 count recall — FDA D-1241-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
GlaxoSmithKline Consumer Healthcare Nicorette Lozenge and NicoDerm CQ, nicotine polacrilex recall — FDA D-1247-2014
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Class IIIFDA: TerminatedGlaxoSmithKline Consumer Healthcare;…
DrugApr 30, 2014
Brookfield Prescription Center Glycopyrrolate (MDV) 0.2 MG/ML Injectable, 5 mL Vials recall — FDA D-1252-2014
Non-Sterility: One lot of Glycopyrrolate solution for injection was found to be contaminated with Bacillus thuringiensis.
Class IFDA: TerminatedBrookfield Prescription Center Inc.
DrugApr 30, 2014
LORATADINE AND PSEUDOEPHEDRINE SULFATE Non-Drowsy 24 Hour Formula Allergy Relief and Nasal recall — FDA D-1256-2014
Defective Container: An unacceptable level of blister defects have been identified in Loratadine and Pseudoephedrine Sulfate Extended Release Tablets, 10 mg/240 mg.
Class IIFDA: TerminatedOhm Laboratories, Inc.
DrugApr 30, 2014
Hospira Potassium Chloride for Inj recall — FDA D-1261-2014
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
Class IIFDA: TerminatedHospira Inc.
FoodApr 23, 2014
Helados La Tapatia Mango Milk Bars, 3 oz recall — FDA F-1798-2014
FDA environmental sampling found 21 of 50 positive for Listeria monocytogenes, 11 of these on food contact surfaces.
Class IIFDA: TerminatedHelados La Tapatia, Inc.
FoodApr 23, 2014
Clif Bar And Company Luna Chocolate Chunk recall — FDA F-1825-2014
Chocolate Chunk Luna Bars made with macadamia nut butter but macadamia nuts are not included in the ingredient listing or allergen statement.
Class IIFDA: TerminatedClif Bar And Company
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.