Recalls of antidepressants, anti-anxiety and related psychiatric medications.
226 recalls in this category, newest first.
Reason Failed Dissolution Specifications: Stability results found the product did not meet the drug release dissolution specifications.
Reason Failed Dissolution Specifications: Stability results found the product did not meet the drug release dissolution specifications.
Reason Presence of Foreign Tablets/Capsules: report of a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule was found…
Reason Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule…
Reason Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg &…
Reason Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg &…
Reason Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg &…
Reason Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Reason Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual…
Reason Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor.
Reason Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor.
Reason Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.
Reason Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.
Reason Failed Dissolution Specifications: Failed stability testing for dissolution test at 18 months.
Reason Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification.
Reason Labeling: Incorrect or Missing Lot No. and/or Exp Date: Expiration date incorrectly reflects a 36 month shelf life, instead of the 24 month shelf life
Reason Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets
Reason Failed Dissolution Specification:12 hour time point at 18 months of product shelf life.
Reason Failed Dissolution Specifications: This recall is an extension of the recall initiated on 07/31/2013 for Bupropion HCl Extended-Release Tablets (XL)…
Reason Failed Dissolution Specifications: Dissolution test results at 8 hour time-point were above approved specification limits.
Reason Labeling: Label Mixup: VENLAFAXINE HCL ER, Capsule, 150 mg may have potentially been mislabeled as one of the following drugs: SOTALOL HCL, Tablet…
Reason Labeling: Label Mixup: VENLAFAXINE HCL, Tablet, 100 mg may have potentially was mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915…
Reason Labeling: Label Mixup: VENLAFAXINE HCL, Tablet, 75 mg may have potentially been mislabeled as the following drug: TACROLIMUS, Capsule, 1 mg, NDC…
Reason Labeling: Label Mixup: ESCITALOPRAM, Tablet, 5 mgmay have potentially been mislabeled as the following drug: SODIUM CHLORIDE, Tablet, 1 gm, NDC…
Reason Labeling: Label Mixup: clonazePAM, Tablet, 0.25 mg (1/2 of 0.5 mg) may have potentially been mislabeled as the following drug: CHOLECALCIFEROL…
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