Complete FDA and NHTSA recall records dated in 2014, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Marketed Without an Approved NDA/ANDA; Product contains undeclared indomethacin, diclofenac, and chlorzoxazone.
Failed pH Specification: A pH result of 2.9 was obtained at the 9 month stability test interval at 25C/60%RH. The registered specification for pH is 3.0 - 7.0
Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa and Levodopa Tablets USP, 25mg/100mg due to the potential for superpotent tablets.
Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
Marketed Without an Approved NDA/ANDA: Bacai, Inc. DBA Ky Duyen House is voluntarily recalling Lite Fit USA, lot 13165, due to undeclared sibutramine, making it an unapproved new drug.
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
Beirut Lift Turnip Pickles contains undeclared FD & C Red #40 and unallowable dye 45170 Rhodamine B - Basic Violet 10.
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
Recent tests show that the "Simply Enjoy Chocolate Chip Walnut Cookies", Use by date Nov 5 2014, contain undeclared Macademia Nuts which could run the risk of serious or life-threatening…
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
Milk Specialties Global is recalling 2 lots of MuscleTech Amino Build Fruit Punch due to potential cross contamination with egg protein.
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
The firm is recalling all lots of the following products due to the potential presence of peanut protein: Kind Maple Pumpkin Baked Bar,Strong & Kind Honey Mustard, Strong & Kind Thai Sweet…
Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.
Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA as a drug manufacturer
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
