FDA Drug recall D-1065-2014
Namenda XR (memantine HCl), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only, Forest Pharmaceutical…
- FDA Drug
- Class III
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class III recall of Namenda XR (memantine HCl), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only, Forest Pharmaceutical… by Forest Pharmaceuticals, citing failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1065-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-11-13 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Forest Pharmaceuticals |
| Distribution | US |
Product
Namenda XR (memantine HCl), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045 NDC 0456-3428-05.
Reason
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Identifiers
| code_info | Lot 1112467 Exp. 02/15 |
|---|
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-1065-2014%22
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