95,025 total recalls in our database
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
The firm was notified by a customer that the label does not declare pecans in its ingredient statement.
Doux South Specialties
The firm received a positive test result for Listeria monocytogenes for the product.
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
R & S Roberts Enterprises
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
Subpotent drug: Low OOS for menthol content at the three month room temperature.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
Microbial Contamination of Non-Sterile Products
Microbial Contamination of Non-Sterile Products
CGMP Deviations: Failure to properly investigate failed microbial testing.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
CGMP Deviations: Failure to properly investigate failed microbial testing.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
CGMP Deviations: Failure to properly investigate failed microbial testing.