Ascend Laboratories, LLC — FDA Class II (D-0547-2026)

Ascend Laboratories, LLC is recalling 17,304 bottles of a human prescription drug due to failed dissolution specifications. This recall is classified as a safety issue. The affected products have NDC numbers 67877-590, 67877-591, 67877-592, and 67877-593.

• •Ascend Laboratories is recalling 17,304 bottles of a human prescription drug.
• •The recall is due to failed dissolution testing.
• •Affected products have NDC numbers 67877-590 to 67877-593.
• •Patients should check their medicine cabinets for these products.
• •This recall is classified as a Class II safety issue.

Patients using these drugs should stop immediately and consult their healthcare provider. The recall affects 17,304 bottles distributed nationwide.