Recalls of ARBs, ACE inhibitors, beta blockers and other hypertension drugs - the class behind the large valsartan and losartan nitrosamine recalls.
548 recalls in this category, newest first.
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Reason Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Reason Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Reason Failed tablet/capsule specification: missing break line on the 5mg tablet.
Reason Presence of Foreign Tablets/Capsules
Reason Presence of Foreign Tablets/Capsules
Reason Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect lot number, 327B160012, appears on the case label, the correct lot number, 327B16002…
Reason Labeling: Incorrect or Missing Package Insert
Reason CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Reason CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Reason CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Reason Lack of Processing Controls
Reason Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.
Reason CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Reason CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Reason Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)
Reason Failed Impurities/Degradation Specifications; 9 month stability timepoint
Reason Presence of Particulate Matter
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