Class II · Moderate risk Ongoing
Desmopressin Nasal Spray
Reason Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
Desmopressin Acetate Tablets
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
What was recalled
Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.
- Recalling firm
- American Health Packaging
- Origin
- OH, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1235-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Desmopressin recalls
See all
Class II · Moderate risk Terminated
Desmopressin Acetate Tablet
Reason Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Class II · Moderate risk Terminated
Desmopressin Acetate Tablets 0.2mg
Reason Subpotent Drug
Class II · Moderate risk Terminated
Desmopressin Acetate Tablets
Reason CGMP Deviations
Class II · Moderate risk Terminated
Desmopressin Acetate Injection USP
Reason Lack of Assurance of Sterility: manufacturing areas for the recalled products exceeded acceptance levels for microbial recovery leading to a lack of sterility assurance for these sterile injectable products.
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