FoodFeb 8, 2017
Raley's recall — FDA F-1426-2017
In response to a consumer complaint, Investigation by the manufacturer determined that a partial black rat was found in the product.
Class IIFDA: TerminatedRaley's
Monthly breakdown
2017 recalls by month
Select a month to review the recall records reported during that period.
December 2017183 records · 3 categoriesNovember 2017262 records · 2 categoriesOctober 201750 records · 2 categoriesSeptember 2017124 records · 2 categoriesAugust 2017178 records · 2 categoriesJuly 2017212 records · 2 categoriesJune 2017121 records · 3 categoriesMay 2017245 records · 3 categoriesApril 2017306 records · 2 categoriesMarch 2017226 records · 2 categoriesFebruary 2017106 records · 2 categoriesJanuary 2017396 records · 2 categories
2017 recalls — page 83
Records are ordered by the best available source date.
FoodFeb 8, 2017
Rich Products KEEP FROZEN, UNIT NET WT: 60 OZ recall — FDA F-1366-2017
The product may contain undeclared walnuts from intermediate layer cake supplier.
Class IIFDA: TerminatedRich Products Corp
FoodFeb 8, 2017
Rich Products Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CAKE recall — FDA F-1365-2017
The product may contain undeclared walnuts from intermediate layer cake supplier.
Class IIFDA: TerminatedRich Products Corp
DrugFeb 8, 2017
CARBIDOPA AND LEVODOPA Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) recall — FDA D-0455-2017
Failed Dissolution Specifications
Class IIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugFeb 8, 2017
VistaPharm Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 recall — FDA D-0457-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
Finasteride Tablets, USP 5 mg, 90-count bottles recall — FDA D-0453-2017
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
Class IIIFDA: TerminatedHetero Drugs Ltd. - Unit 1
DrugFeb 8, 2017
Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a.) 1 fl. oz. (30 mL), 12 recall — FDA D-0465-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II (Sugar Free), 1 liter (1000 mL) recall — FDA D-0466-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
Ecolab Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution, 4% recall — FDA D-0454-2017
Subpotent Drug
Class IIIFDA: TerminatedEcolab, Inc.
DrugFeb 8, 2017
VistaPharm Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL, a). 5 mL, 50 unit dose cups recall — FDA D-0464-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Phenytoin Oral Suspension, USP 100 mg/ 4 mL, 50 unit dose cups of 4 mL per case recall — FDA D-0460-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles recall — FDA D-0467-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/325 mg per 15 mL recall — FDA D-0458-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL recall — FDA D-0461-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Lactulose Solution, USP 20 g/30 mL, 50 unit dose cups of 30 mL per case recall — FDA D-0462-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Lactulose Solution, USP 10 g/15 mL, 50 unit dose cups of 15 mL per case recall — FDA D-0463-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
DrugFeb 8, 2017
VistaPharm Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per recall — FDA D-0459-2017
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Class IIFDA: TerminatedVistaPharm, Inc.
FoodFeb 1, 2017
Victory General Foods ELDER PAINTSIL'S FANTE KENKEY, NET WT recall — FDA F-1336-2017
Product manufactured under insanitary conditions and firm did not follow the Food Code-mandated scheduled process
Class IIFDA: TerminatedVictory General Foods Inc.
FoodFeb 1, 2017
Coca-Cola Consolidated Dr recall — FDA F-1344-2017
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).
Class IIIFDA: TerminatedCoca-Cola Consolidated
FoodFeb 1, 2017
Berner Food & Beverage Four Cheese Alfredo, Pasta Sauce recall — FDA F-1358-2017
Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Class IIFDA: TerminatedBerner Food & Beverage, LLC
FoodFeb 1, 2017
Authentic Alaska Alaska Salmon Bites recall — FDA F-1334-2017
Alaska Salmon Bites (jerky), Spicy Fireweed Honey flavor is recalled due to undeclared soy. Product contains undeclared soy sauce from the ingredient Tamari sauce.
Class IIFDA: TerminatedAuthentic Alaska
FoodFeb 1, 2017
Boulder Brands Earth Balance Vegan White Cheddar flavored Mac and Cheese, 6oz recall — FDA F-1361-2017
Earth Balance Vegan White Cheddar flavored Mac and Cheese and Earth Balance Vegan Cheddar flavored Mac and Cheese with undeclared allergen, milk.
Class IFDA: TerminatedBoulder Brands, LLC
FoodFeb 1, 2017
Farm to Market Foods Green Bean Casserole Code #1958 Net Wt recall — FDA F-1340-2017
Undeclared peanuts.
Class IIFDA: TerminatedFarm To Market Foods
FoodFeb 1, 2017
Tortillas Tita 18 Count-16 Oz./453 g 16 units per case, 10 Count- 8 Oz./283 g recall — FDA F-1354-2017
Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.
Class IIFDA: TerminatedTortillas Tita, LLC
About the 2017 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.