Drug recall
Glipizide XL (glipizide) extended release tablets, 5 mg, 500 count bottles, Rx only, Distributed by…
FDA recall event 66814 · Class III · Greenstone Llc
Key facts
| Event ID | 66814 |
|---|---|
| Recall numbers | D-1059-2014 |
| Recalling firm | Greenstone Llc |
| Product type | Drugs |
| Products | Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ --- NDC 59762-5032-2 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval |
| Initiation date | Nov 4, 2013 |
| Report date | Feb 12, 2014 |
| Termination date | Jun 24, 2015 |
| City | Peapack |
| State | NJ |
| Country | United States |
| FEI number | 3008196528 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: