Class III โ€” Low Risk

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

Glipizide XL (glipizide) extended release tablets Recalled by Greenstone Llc Due to Failed Dissolution Specification; the bulk lot yielded an...

Date: November 4, 2013
Company: Greenstone 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 Greenstone Llc directly.

Affected Products

Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ --- NDC 59762-5032-2

Quantity: 22,529 bottles

Why Was This Recalled?

Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Greenstone Llc

Greenstone Llc has 6 total recalls tracked by RecallDetector.

Related Recalls

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