FoodAug 27, 2014
The TJX Companies Product is in a 160 gram, light green tin container, labeled recall — FDA F-2333-2014
Salmonella
Class IFDA: TerminatedThe TJX Companies, Inc.
Recall records from August 2014
These records include useful source details for the selected month.
FoodAug 27, 2014
American Spoon Foods 9.5 oz in glass jars with metal lid e recall — FDA F-2343-2014
Product may have mold in jar.
Class IIFDA: TerminatedAmerican Spoon Foods, Inc.
FoodAug 27, 2014
FISH FAMILY FARM INC recall — FDA F-2346-2014
Milk products and cream products may be contaminated with peanuts and tree nuts (pistachio).
Class IIFDA: TerminatedFish Family Farm
FoodAug 27, 2014
Renfro Foods XOCHITL recall — FDA F-2341-2014
Undeclared wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.
Class IIFDA: TerminatedRenfro Foods, Inc.
FoodAug 27, 2014
CaCoCo Superfood Drinking Chocolate recall — FDA F-2337-2014
Firm used organic powder that is now under recall by supplier for potential contamination with Salmonella.
Class IFDA: TerminatedCaCoCo, Inc.
FoodAug 27, 2014
FISH FAMILY FARM INC recall — FDA F-2348-2014
Milk products and cream products may be contaminated with peanuts and tree nuts (pistachio).
Class IIFDA: TerminatedFish Family Farm
FoodAug 27, 2014
FISH FAMILY FARM INC recall — FDA F-2347-2014
Milk products and cream products may be contaminated with peanuts and tree nuts (pistachio).
Class IIFDA: TerminatedFish Family Farm
FoodAug 27, 2014
Natural Grocers by Vitamin Cottage 0.70 lb recall — FDA F-2336-2014
Natural Grocers by Vitamin Cottage is recalling Chunks of Energy Carob Greens and Chunks of Energy Date Flax/Tumeric due to the potential presence of Salmonella.
Class IFDA: TerminatedNatural Grocers by Vitamin Cottage
FoodAug 27, 2014
D.A. Stein Culinary Group, LLC dba Brett Anthony Sesame Ginger Dressing sold under the Whole recall — FDA F-2344-2014
Brett Anthony Foods is recalling Sesame Ginger Dressing because the allergen almonds (a tree nut) is not listed in the "Contains" allergen warning statement although almonds are listed in…
Class IIFDA: TerminatedD.A. Stein Culinary Group, LLC dba Brett Anthony Foods
FoodAug 27, 2014
Natural Grocers by Vitamin Cottage 0.70 lb recall — FDA F-2335-2014
Natural Grocers by Vitamin Cottage is recalling Chunks of Energy Carob Greens and Chunks of Energy Date Flax/Tumeric due to the potential presence of Salmonella.
Class IFDA: TerminatedNatural Grocers by Vitamin Cottage
FoodAug 27, 2014
Renfro Foods Chile Con Queso recall — FDA F-2342-2014
Undeclared wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.
Class IIFDA: TerminatedRenfro Foods, Inc.
FoodAug 27, 2014
Renfro Foods XOCHITL recall — FDA F-2340-2014
Undeclared wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.
Class IIFDA: TerminatedRenfro Foods, Inc.
FoodAug 27, 2014
Ciranda Product Code 20030 recall — FDA F-2334-2014
Ciranda is recalling one lot of Organic Carob Powder Light after learning that a customer received a positive test for Salmonella.
Class IFDA: TerminatedCiranda, Inc.
FoodAug 27, 2014
FISH FAMILY FARM INC recall — FDA F-2349-2014
Milk products and cream products may be contaminated with peanuts and tree nuts (pistachio).
Class IIFDA: TerminatedFish Family Farm
FoodAug 27, 2014
CaCoCo Superfood Drinking Chocolate recall — FDA F-2338-2014
Firm used organic powder that is now under recall by supplier for potential contamination with Salmonella.
Class IFDA: TerminatedCaCoCo, Inc.
FoodAug 27, 2014
FISH FAMILY FARM INC recall — FDA F-2345-2014
Milk products and cream products may be contaminated with peanuts and tree nuts (pistachio).
Class IIFDA: TerminatedFish Family Farm
DrugAug 27, 2014
ProSol - sulfite-free (Amino Acid) Injection, 20%, 2000 mL VIAFLEX container bag recall — FDA D-1542-2014
Presence of Particulate Matter: identification of particulates in a retention sample that have been identified as a mixture of the amino acid leucine and inorganic material (containing…
Class IIFDA: TerminatedBaxter Healthcare Corp
DrugAug 27, 2014
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), For I.V recall — FDA D-1547-2014
Presence of Particulate Matter: A glass defect was found on the interior neck of the vial during a retain sample inspection where the glass vial contained visible embedded metallic…
Class IFDA: TerminatedHospira Inc.
DrugAug 27, 2014
Healix Infusion Therapy fentaNYL 200 mcg/100 mL (2 mcg/mL) and Ropivacaine 0.2% in 0.9% recall — FDA D-1553-2014
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.
Class IIFDA: TerminatedHealix Infusion Therapy, Inc.
DrugAug 27, 2014
Healix Infusion Therapy fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED recall — FDA D-1554-2014
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.
Class IIFDA: TerminatedHealix Infusion Therapy, Inc.
DrugAug 27, 2014
US Compounding ePHEDrine Sulfate Injection, USP 25 mg/5 mL (5 mg/mL) Single Use 5 mL recall — FDA D-1548-2014
Labeling: Label Error on Declared Strength; The outer light protective bags, where the ephedrine sulfate injection syringes are stored, were mislabeled with 25 mg/mL in big font and 5 mg/mL…
Class IIFDA: TerminatedUS Compounding Inc.
DrugAug 27, 2014
Trigen Laboratories Triveen - PRx RNF Capsules, 30-count bottles recall — FDA D-1544-2014
Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on the Supplement Facts panel, however, the formulation of this product does not…
Class IIIFDA: TerminatedTrigen Laboratories, Inc.
DrugAug 27, 2014
Healix Infusion Therapy fentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride in recall — FDA D-1552-2014
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.
Class IIFDA: TerminatedHealix Infusion Therapy, Inc.
DrugAug 27, 2014
Ben Venue Laboratories CYTARAbine for Injection USP, lyophiled in glass vials, 1 gram per recall — FDA D-1543-2014
Lack of Assurance of Sterility: Crimp defects during visual inspection could affect container closure integrity.
Class IIFDA: TerminatedBen Venue 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.