All Recalls

Products may be contaminated with peanut protein.

The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is recalling all items produced on the filling line between sanitation cycles.

Kale Crisps Lemon Parmesan is recalled because label declared Parmesan cheese but milk is not declared.

The firm failed to declare the allergen eggs on their labels.

The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is recalling all items produced on the filling line between sanitation cycles.

The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is recalling all items produced on the filling line between sanitation cycles.

The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is recalling all items produced on the filling line between sanitation cycles.

Vegetable Crisps Lemon Parmesan is recalled because label declared Parmesan cheese but milk is not declared.

One lot of Vic's Original White Popcorn 1-1/8oz size bags contains an undeclared milk allergen. White Cheddar Popcorn, a product containing milk, was distributed in packaging for a different product, Original White Popcorn.

Nepali Finger Chips contains undeclared tartrazine (yellow #5).

A bag of Fisher Walnuts sampled by the FDA, tested positive for Salmonella.

Products may be contaminated with peanut protein.

Kale Crisps Zen Nori is recalled due to undeclared SOY. Soybean is a sub-ingredient of the ingredient "Tamari" and soy is not declared on label.

The firm failed to declare the allergen eggs on their labels.

Failed Impurities/Degradation Specifications: out-of-specification results for individual unknown and total impurity at the 12th month room temperature stability test station

Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.

Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.

Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.

Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were subsequently recalled by the manufacturer due to the presence of particulate matter.

Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.