Morrison's cornbread dressing packaged in 7lb trays
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
95,038 total recalls in our database
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
The cheese ingredient used in the product tested positive for Listeria monocytogenes.
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
The outer retail packaging claims "Gluten Free" but the inner individual pouch declares wheat.
The cheese ingredient used in the product tested positive for Listeria monocytogenes.
AQUABEST SEAFOOD
Product recalled due to potentially elevated levels of Histamines. Product supplier, TPX, is recalling product which is related to a recent scombrotoxin poisoning outbreak in US.
Savannah Food Company
Eggs used in the manufacture of the products may be contaminated with listeria monocytogenes
The outer retail packaging claims "Gluten Free" but the inner individual pouch declares wheat.
AQUABEST SEAFOOD
Product recalled due to potentially elevated levels of Histamines. Product supplier, TPX, is recalling product which is related to a recent scombrotoxin poisoning outbreak in US.
Tuscano and Delucia Group (DBA Entropic Labs)
Marketed Without An Approved NDA/ANDA: product contains Selective Androgen Receptor Modulators (SARMs)
Mylan Pharmaceuticals
CGMP Deviations: Trace amounts of an impurity, N-nitrosodimethylamine (NDMA) was detected in the API Nizatidine.
CGMP Deviations: Presence of NDMA impurity detected in product.
CGMP Deviations: Presence of NDMA impurity detected in product.
Hikma Pharmaceuticals USA
Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.
Mylan Pharmaceuticals
CGMP Deviations: Trace amounts of an impurity, N-nitrosodimethylamine (NDMA) was detected in the API Nizatidine.
RemedyRepack
CGMP Deviation; Received notice from supplier of potential -Nitrosodimethylamine (NDMA) amounts above established levels.
Advanced Accelerator Applications USA
Defective Container: loose aluminum cap crimp for the dilution buffer vial present in the NETSPOT Kit (vial 2).
CGMP Deviations: Presence of NDMA impurity detected in product.