10 FDA recalls mention Citalopram. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Citalopram.
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
Reason Lack of Processing Controls
Reason Labeling: Incorrect or Missing Lot and/or Expiration Date
Reason Penicillin Cross Contamination: All lots of all products repackaged between 01/05/12 through 02/12/15 are being recalled because they were repackaged…
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; CITALOPRAM Tablet, 10 mg may be potentially mislabeled as OXYBUTYNIN CHLORIDE, Tablet, 5 mg, NDC 00603497521, Pedigree…
Reason Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
Reason Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
Reason Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
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