Desmopressin Acetate Tablets 0.2mg
Subpotent Drug
Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.
14,535 recalls, newest first.
Subpotent Drug
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
CGMP Deviations: Potential for cross contamination due to product carry over.
CGMP Deviations: Potential for cross contamination due to product carry over.
Failed Impurities/Degradation Specifications
CGMP deviations
Lack of assurance of sterility: Bags have the potential to leak in the flexible containers which may compromise sterility.
Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.
CGMP Deviations: Other lots of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
cGMP deviation: discontinue of stability support for product.
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.
Presence of Foreign Substance
CGMP Deviations:
CGMP Deviations:
CGMP Deviations:
CGMP Deviations:
CGMP Deviations:
CGMP Deviations:
CGMP Deviations:
CGMP Deviations: