31 FDA recalls mention Venlafaxine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Venlafaxine.
Reason Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet.
Reason Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Reason Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
Reason Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
Reason Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Reason Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Reason Failed Dissolution Specifications: Out-of-specification results in retained sample.
Reason Failed Dissolution Specifications: Out-of-specification results in retained sample.
Reason Failed Dissolution Specifications: out of specification dissolution results in retained samples
Reason Failed Dissolution Specifications: out of specification dissolution results in retained samples
Reason Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as…
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 Dissolution Specifications; 12 month stability time point
Reason Failed Dissolution Specifications: Stability results found the product did not meet the drug dissolution specifications.
Reason Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq (desvenlafaxine) extended release tablets because a single Pristiq 100 mg…
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 Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Reason Failed Dissolution Specification:12 hour time point at 18 months of product shelf life.
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…
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