FDA Drug recall D-1235-2015
Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons
- FDA Drug
- Class III
- terminated
- Published 2015-07-22
On 2015-07-22 the FDA classified a Class III recall of Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons by American Health Packaging, citing tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1235-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-06-26 |
| Published | 2015-07-22 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | American Health Packaging |
| Distribution | US |
Product
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.
Reason
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Identifiers
| code_info | Lot #:151360, Expiry: 12/31/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1235-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.