All Recalls

Whole Foods Market is recalling CC & FP HSH Coconut Curry Cauliflower Salad because an undeclared allergen, almonds, was mistakenly included in the salad kit.

Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.

Ajinomoto Windsor is recalling various Not-Ready-To Eat frozen food items due to the potential for these products to be contaminated with Listeria monocytogenes.

The product may contain foreign material (glass) in some bottles.

Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.

Undeclared peanuts in fully-baked cookies.

Lack of assurance of sterility: This recall includes of all unexpired lots medications containing Calcium Gluconate, Papaverine, Phentolamine, and /or Prostaglandin) due to unsubstantiated validation of beyond use dating.

Lack of assurance of sterility: This recall includes of all unexpired lots medications containing Calcium Gluconate, Papaverine, Phentolamine, and /or Prostaglandin) due to unsubstantiated validation of beyond use dating.

Failed Impurities/Degradation Specifications

Labeling: Label Error on Declared Strength- bottles missing colored coded panel where strength of the product is displayed.

Failed Impurities/Degradation Specifications

CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that product sterility may be compromised.

Lack of assurance of sterility: This recall includes of all unexpired lots medications containing Calcium Gluconate, Papaverine, Phentolamine, and /or Prostaglandin) due to unsubstantiated validation of beyond use dating.

Labeling: Label Error on Declared Strength; label on outer carton incorrectly states Diphenhydramine 25 mg instead of 12.5 mg. Also, quantity is incorrectly stated as 30 daytime and 30 nighttime instead of 36 daytime and 24 nighttime.

Labeling: Incorrect or Missing Lot and/or Expiration Date

CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that product sterility may be compromised.

Failed Impurities/Degradation Specifications

Lack of assurance of sterility: This recall includes of all unexpired lots medications containing Calcium Gluconate, Papaverine, Phentolamine, and /or Prostaglandin) due to unsubstantiated validation of beyond use dating.