16 FDA recalls mention Desmopressin. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Desmopressin.
Reason Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
Reason Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Reason Subpotent Drug
Reason CGMP Deviations
Reason Lack of Assurance of Sterility: manufacturing areas for the recalled products exceeded acceptance levels for microbial recovery leading to a lack of…
Reason Superpotent Drug
Reason Superpotent Drug
Reason Superpotent Drug
Reason GMP Deviations: Product bottle may be absent of desiccant.
Reason GMP Deviations: Product bottle may be absent of desiccant.
Reason GMP Deviations: Product bottle may be absent of desiccant.
Reason GMP Deviations: Product bottle may be absent of desiccant.
Reason Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Reason Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
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 Labeling: Label Mixup: DESMOPRESSIN ACETATE, Tablet 0.1 mg may have potentially been mislabeled as the following drug: LOXAPINE, Capsule, 5 mg, NDC…
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