23 FDA recalls mention Paroxetine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Paroxetine.
Reason Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori…
Reason Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori…
Reason Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori…
Reason Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Reason Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Reason Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Reason Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Reason Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Reason Presence of Foreign Tablets/Capsules.
Reason Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Reason Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.
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 Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and…
Reason Labeling: Label Mixup; PARoxetine HCl, Tablet, 10 mg may be potentially mislabeled as PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, NDC 62175018046…
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