Telmisartan Tablets
Failed Stability Specifications: Out of specification for blend uniformity.
Recalls of ARBs, ACE inhibitors, beta blockers and other hypertension drugs - the class behind the large valsartan and losartan nitrosamine recalls.
549 recalls in this category, newest first.
Failed Stability Specifications: Out of specification for blend uniformity.
Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots
Failed Impurities/Degradation Specifications
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Failed Dissolution Specification
Failed Dissolution Specification
Failed Dissolution Specification
Failed Impurity/Degradation Specifications
Failed Impurity/Degradation Specifications
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Failed Dissolution Specifications
Failed dissolution specifications.
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Subpotent and Superpotent Drug
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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