E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle recall — FDA D-1536-2014
Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
Complete FDA and NHTSA recall records dated in August 2014.
These records include useful source details for the selected month.
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
Failed Tablet/Capsule Specifications: Ink identification had rubbed off tablets in transit making them illegible to pharmacists and consumers.
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
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
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.