Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Enalapril Maleate Tablet Recalled by Apace KY LLC Due to Labeling Illegible: Some bottles labels have incomplete NDC...

Date: September 4, 2012
Company: Apace KY LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Apace KY LLC directly.

Affected Products

Enalapril Maleate Tablet, USP 5mg 30 Tablet bottle, Rx, Apace Packaging LLC, Ft. Run, KY 42133, NDC 15338-211-30

Quantity: 81,516 bottles

Why Was This Recalled?

Labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Apace KY LLC

Apace KY LLC has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report