Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc., Preferred Pharmaceuticals, Inc.
Preferred Pharmaceuticals
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
💊 Drugs • 3,313 recalls
Preferred Pharmaceuticals
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
VIRGIN SCENT
CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
Chemical Contamination: presence of benzene, acetaldehyde, and acetal.
Revive Personal Products Company
Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
Lack of sterility assurance.
Tennessee Technical Coatings
Chemical Contamination: FDA analysis found 1 lot of HAND SANITIZER Isopropyl Alcohol Antiseptic 75%, to contain methanol.
Tennessee Technical Coatings
CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
Labeling: Label Mix-Up-The primary label on the front of the bottles have 50% Isopropyl Alcohol affixed to the containers. However, the product inside the bottle is Hydrogen Peroxide, Topical Solution USP with active ingredient Hydrogen Peroxide (stabilized) 3%, 32 FL Ounces. The back label is correct. Product is packaged in dark bottles.
Labeling - product contains undeclared ethyl alcohol
Labeling - product contains undeclared ethyl alcohol
Perrigo Company PLC
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo Company PLC
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.