FoodJul 23, 2014
New B.C.N. Trading CTF Brand Tapioca Pearl Net Wt: 14 oz recall — FDA F-2172-2014
Tapioca pearl contains unapproved and undeclared colors.
Class IIFDA: TerminatedNew B.C.N. Trading Inc.
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 54
Records are ordered by the best available source date.
FoodJul 23, 2014
NW Nutritional Foods There are two different labels for this product same UPC codes recall — FDA F-2186-2014
Undeclared milk found in bars labeled "dairy free" or "vegan."
Class IIFDA: TerminatedNW Nutritional Foods LLC
FoodJul 23, 2014
NW Nutritional Foods There are three different labels for this product recall — FDA F-2187-2014
Undeclared milk found in bars labeled "dairy free" or "vegan."
Class IIFDA: TerminatedNW Nutritional Foods LLC
FoodJul 23, 2014
Nestle H¿agen-Dazs Chocolate Chocolate Chip Ice Cream, 14 oz, UPC of recall — FDA F-2191-2014
Nestle is recalling the H¿agen-Dazs Chocolate Chocolate Chip Ice Cream because it was mislabeled and the ingredient statement does not identify peanuts. The affected products are labeled as…
Class IFDA: TerminatedNestle
FoodJul 23, 2014
Six Dog Certified Organic, Owl Canyon Whole Eggs, packed in one dozen recall — FDA F-2176-2014
Eggs have the potential to be contaminated with Salmonella Enteritidis
Class IFDA: TerminatedSix Dog, LLC
DrugJul 23, 2014
Fougera Pharmaceuticals Triamcinolone Acetonide Lotion USP, 0.1%, 60 mL Bottle recall — FDA D-1440-2014
Failed PH Specifications: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Class IIIFDA: TerminatedFougera Pharmaceuticals Inc.
DrugJul 23, 2014
Axcentria Pharmaceuticals Hemo-Stat Solution, Aluminum chloride 25%, in 37.2 g glass bottles recall — FDA D-1434-2014
Marketed without an Approved NDA/ANDA; product is being manufactured and distributed without a NDC number
Class IIFDA: TerminatedAxcentria Pharmaceuticals, LLC
DrugJul 23, 2014
Poly Pharmaceuticals POLY-TUSSIN AC LIQUID, Each 5 mL (1 teaspoonful) contains recall — FDA D-1431-2014
Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".
Class IIIFDA: TerminatedPoly Pharmaceuticals, Inc.
DrugJul 23, 2014
Mylan Institutional Diltiazem HCl Extended-release Capsules, USP, 120 mg recall — FDA D-1435-2014
Failed Impurities/Degradation Specifications: High out-of-specification results for a related compound obtained during routine stability testing.
Class IIIFDA: TerminatedMylan Institutional, Inc. (d.b.a. UDL Laboratories)
DrugJul 23, 2014
Poly Pharmaceuticals LORTUSS EX, Each 5 mL (1 teaspoonful) contains: Codeine Phosphate 10 recall — FDA D-1432-2014
Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".
Class IIIFDA: TerminatedPoly Pharmaceuticals, Inc.
DrugJul 23, 2014
Fougera Pharmaceuticals Triamcinolone Acetonide Lotion USP, 0.025%, 60 mL Bottle recall — FDA D-1441-2014
Failed PH Specifications: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Class IIIFDA: TerminatedFougera Pharmaceuticals Inc.
DrugJul 23, 2014
CareFusion 213 ChloraPrep With Tint, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v recall — FDA D-1442-2014
Lack of Assurance of Sterility; Immediate product pouches may not be properly sealed.
Class IIFDA: TerminatedCareFusion 213, LLC
DrugJul 23, 2014
VIRACEPT (R) (nelfinavir mesylate) Tablets, 625 mg, 120-count bottle recall — FDA D-1443-2014
Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled with an incorrect expiry date 11/2016. The correct expiry date is 09/2016.
Class IIIFDA: TerminatedPfizer Inc.
FoodJul 16, 2014
Modern Macaroni Co Hula Brand Products recall — FDA F-2090-2014
FDA sample 466576 found 208.46 ppm of Sulfites in Hana Ebi dried shrimp product.
Class IIIFDA: TerminatedModern Macaroni Co Ltd
FoodJul 16, 2014
Koogee-Queen Anne Sister Bean's White Chocolate Mocha Ice Cream, Manufactured recall — FDA F-2168-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Banana Walnut Fudge Ice Cream, Manufactured by: Koogee-Queen recall — FDA F-2119-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Hazelnut Crunch Ice Cream, Manufactured by: Koogee-Queen Anne recall — FDA F-2136-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Surma Distributors HAQUE brand GOLDEN RAISINS, WT 7 OZ recall — FDA F-2170-2014
The product was found to contain undeclared sulfites (1329.2 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.
Class IFDA: TerminatedSurma Distributors LLC
FoodJul 16, 2014
Koogee-Queen Anne Green Apple Sorbet, Manufactured by: Koogee-Queen Anne, LLC recall — FDA F-2135-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne S'mores Ice Cream, Manufactured by: Koogee-Queen Anne, LLC recall — FDA F-2147-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Chocolate "Chip Off the Old Block" Ice Cream, Manufactured by recall — FDA F-2164-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Cookie Monster Dough Ice Cream, Manufactured by: Koogee-Queen recall — FDA F-2158-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Old 502 Sangria Ice Cream recall — FDA F-2112-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
FoodJul 16, 2014
Koogee-Queen Anne Coconut Almond Bliss Ice Cream recall — FDA F-2104-2014
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products.…
Class IIFDA: TerminatedKoogee-Queen Anne, LLC
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.