Recalls / Class III
Class IIID-1063-2014
Product
Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045, NDC 0456-3407-33
- Affected lot / code info
- Lot 1111291 Exp. 02/16
Why it was recalled
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Recalling firm
- Firm
- Forest Pharmaceuticals Inc
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 13600 Shoreline Dr, Earth City, Missouri 63045
Distribution
- Quantity
- 156 bottles
- Distribution pattern
- Nationwide and Puerto Rico.
Timeline
- Recall initiated
- 2013-11-13
- FDA classified
- 2014-02-04
- Posted by FDA
- 2014-02-12
- Terminated
- 2014-05-07
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1063-2014. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.