FoodJun 8, 2016
Liquid Assets Angel Wings Complete Daily Multi with 146 nutrients including recall — FDA F-1405-2016
Dietary Supplements contain undeclared milk and soy.
Class IFDA: TerminatedLiquid Assets Inc.
June 2016 recalls — page 5
These records include useful source details for the selected month.
FoodJun 8, 2016
Frank L Harter & Sons SPINACH DIP ING: VEGETABLE SOUP MIX, MAYONAISE, SOUR CREAM recall — FDA F-1315-2016
The firm failed to include the allergens, Milk and Soy, on the label.
Class IFDA: TerminatedFrank L Harter & Sons Inc.
FoodJun 8, 2016
Giant Eagle Pecan Tassie - 6 Pack PLU# 77997 Net Wt recall — FDA F-1409-2016
Giant Eagle discovered that the scale label fails to declare the milk ingredient. The allergen statement does not declare the milk allergen.
Class IFDA: TerminatedGiant Eagle, Inc.
FoodJun 8, 2016
O'Steen Meat Specialties Code 2013 Spicy Mac & Cheese Bites Breaded Macaroni & Monterey recall — FDA F-1412-2016
Potential plastic inclusion.
Class IIFDA: TerminatedO'Steen Meat Specialties, Inc.
FoodJun 8, 2016
Frank L Harter & Sons HAWAIIAN DELIGHT ING: IMITATION SOUR DRESSING, PEACHES recall — FDA F-1314-2016
The firm failed to include the allergens, Milk and Soy, on the label.
Class IFDA: TerminatedFrank L Harter & Sons Inc.
FoodJun 8, 2016
The Kroger Co Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT recall — FDA F-1415-2016
The firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedThe Kroger Co
FoodJun 8, 2016
Liquid Assets Life's Qik Fix 70 Plant Minerals Plus 80 Additional Nutrients recall — FDA F-1406-2016
Dietary Supplements contain undeclared milk and soy.
Class IFDA: TerminatedLiquid Assets Inc.
FoodJun 8, 2016
The Kroger Co Kroger CRANBERRY DELIGHT TRAIL MIX NET WT 14 OZ INGREDIENTS recall — FDA F-1414-2016
The firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedThe Kroger Co
FoodJun 8, 2016
Ouhlala Gourmet Fruit Tartlets, lemon flavor, 9 - 0.53oz recall — FDA F-1419-2016
Products contain undeclared milk on finished product labeling
Class IIFDA: OngoingOuhlala Gourmet LLC
FoodJun 8, 2016
Frank L Harter & Sons PASTA SALAD ING: PASTA, ITALIAN DRESSING, DRY ONIONS, PARSLEY recall — FDA F-1316-2016
The firm failed to include the allergens, Milk and Soy, on the label.
Class IFDA: TerminatedFrank L Harter & Sons Inc.
FoodJun 8, 2016
Bridgewell Resources Ivory Teff Flour, bulk 25 lb bags recall — FDA F-1411-2016
Ivory Teff Flour, Bulk 25 lb. bags, is recalled due to a potential contamination with Salmonella.
Class IFDA: TerminatedBridgewell Resources LLC
FoodJun 8, 2016
The Kroger Co Kroger SALTED SUNFLOWER KERNELS 6 oz recall — FDA F-1416-2016
The firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedThe Kroger Co
FoodJun 8, 2016
Ouhlala Gourmet Fruit Tartlets, Raspberry flavor, 9 - 0.56oz recall — FDA F-1420-2016
Products contain undeclared milk on finished product labeling
Class IIFDA: OngoingOuhlala Gourmet LLC
FoodJun 8, 2016
Giant Eagle Walnut Delights 6 Pack Net Weight: 9 oz recall — FDA F-1408-2016
Giant Eagle discovered that the scale label fails to declare the milk ingredient. The allergen statement does not declare the milk allergen.
Class IFDA: TerminatedGiant Eagle, Inc.
DrugJun 8, 2016
Taro Pharmaceuticals U.S.A ¿Topicort (desoximetasone) Cream USP, 0.05% recall — FDA D-0950-2016
Subpotent Drug
Class IIIFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugJun 8, 2016
Lupin Pharmaceuticals Ceftriaxone for Injection USP, 250 mg, Single Use Vial recall — FDA D-0951-2016
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJun 8, 2016
Lupin Pharmaceuticals Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient, DMF recall — FDA D-0955-2016
CGMP Deviations: active pharmaceutical ingredient intermediates failed specifications.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJun 8, 2016
Lupin Pharmaceuticals Ceftriaxone for Injection USP, 1 g, Single Use Vial (NDC 68180-633-01) recall — FDA D-0953-2016
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJun 8, 2016
Lupin Pharmaceuticals Ceftriaxone for Injection USP, 500 mg, Single Use Vial recall — FDA D-0952-2016
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJun 8, 2016
Lupin Pharmaceuticals Ceftriaxone for Injection USP, 2 g, Single Use Vial (NDC 68180-644-01) recall — FDA D-0954-2016
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
FoodJun 1, 2016
Nubreed Nutrition Undisputed , all lot codes, Flavors: Mango Orange , 330 grams recall — FDA F-1389-2016
Nubreed Nutrition, Inc. is voluntarily recalling all lot codes of multiple flavor varieties of the dietary supplement "UNDISPUTED" because it contains the ingredient Acacia rigidula which…
Class IIFDA: TerminatedNubreed Nutrition, Inc.
FoodJun 1, 2016
THE SAUSAGE MAKER SEASONING Summer Sausage under the following recall — FDA F-1381-2016
Fermento ingredient contains undeclared whey protein and skim milk powder
Class IFDA: TerminatedThe Sausage Maker, Inc.
FoodJun 1, 2016
THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the recall — FDA F-1377-2016
Fermento ingredient contains undeclared whey protein and skim milk powder
Class IFDA: TerminatedThe Sausage Maker, Inc.
FoodJun 1, 2016
THE SAUSAGE MAKER SEASONING Dried Sticks Hot under the recall — FDA F-1378-2016
Fermento ingredient contains undeclared whey protein and skim milk powder
Class IFDA: TerminatedThe Sausage Maker, 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.