FDAFDA · Food and drugs·Recall number D-1059-2014
Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ --- NDC 59762-5032-2
Published February 12, 2014 · Recall initiated: November 4, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Greenstone Llc
- Distributor
- US Nationwide (including PR)
- Lot
- lot V112000, EXP Jun 2016
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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