Regency Group, Inc., The Taco Seasoning No Salt, stock code 03455, packaged in 1 lb., 2 recall — FDA F-2337-2015
Taco Seasoning No Salt is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
Complete FDA and NHTSA recall records dated in June 2015.
These records include useful source details for the selected month.
Taco Seasoning No Salt is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
This voluntary recall has been initiated because Conway Import Co.'s Citrus Vinaigrette and Organic Sesame Ginger may contain Salmonella.
French Fry Seasoning is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
The Santa Barbara Smokehouse, Inc. is recalling lot #1894 of Channel Island Old Fashioned Smokehouse Smoked Atlantic Salmon due to potential Listeria monocytogenes contamination.
Product has the potential to be contaminated with Listeria monocytogenes.
Fajita Seasoning is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
Fresca Tomato Spice with Beet is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
Bulk ground oregano is recalled due to contamination with gluten (wheat allergen)
cGMP Deviations; products being recalled in response to a recall notice from the manufacturer, Wockhardt Limited, following a FDA inspection which noted inadequate investigation of market…
Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200 mg/mL in Sesame Oil are being recalled because they contains Estradiol Valerate 20 mg/mL.
Subpotent Drug: The firm received an out of specification result for Assay (potency was below specification) at the 9 month stability time point.
Failed Impurities/Degradation Specifications: out of specification test results for an impurity during stability testing.
cGMP Deviations; products being recalled in response to a recall notice from the manufacturer, Wockhardt Limited, following a FDA inspection which noted inadequate investigation of market…
Non-Sterility: Confirmed customer report of dark, fibrous particulates floating within the solution of the primary container, which were subsequently identified as mold
Defective Delivery System: One lot exceeded the mechanical peel specification
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.