Desmopressin Acetate Tablets, 0.2 mg, 30 tablets (3 x 10 unit dose blister cards), Rx Only, Packaged and distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-604-21; NDC Unit Dose 68084-604-11
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot 180510, exp 3/31/2020; Lot 181912, exp 4/30/2020
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- American Health Packaging
- Reason for Recall:
- GMP Deviations: Product bottle may be absent of desiccant.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Desmopressin Acetate Tablets, 0.2 mg, 30 tablets (3 x 10 unit dose blister cards), Rx Only, Packaged and distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-604-21; NDC Unit Dose 68084-604-11
Product Codes/Lot Numbers:
Lot 180510, exp 3/31/2020; Lot 181912, exp 4/30/2020
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0849-2020
Related Recalls
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Subpotent Drug: Out of specification for assay.
Impurity failure at 0-time of the repackaged lot.