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 Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.
Reason Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.
Reason Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.
Reason Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.
Reason Failed Impurities/Degradation Specifications: An Out of Specification (OOS) result was generated for the 18 month stability time point for ketone…
Reason Discoloration: Brown spots were noted embedded in Amlodipine Besylate Tablets, 10 mg, Lot # MP4344.
Reason Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
Reason Failed Impurity/Degradation Specification; high out of specification for CAD II degradant
Reason Superpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeably thicker in appearance.
Reason Failed Dissolution Specifications: Dissolution failures found during testing of control samples at the four hour time point.
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Reason Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Reason Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Reason Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet of different size and markings in bottle of Metoprolol
Reason Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.
Reason Labeling: Incorrect or Missing Package Insert: Product is packaged with the incorrect version of the package insert.
Reason Labeling: Incorrect or Missing Package Insert: Product is packaged with the incorrect version of the package outset
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