Drug recall
Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only…
FDA recall event 67747 · Class III · McKesson Packaging Services
Key facts
| Event ID | 67747 |
|---|---|
| Recall numbers | D-1167-2014 |
| Recalling firm | McKesson Packaging Services |
| Product type | Drugs |
| Products | Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA, 1090 Horsham Rd, North Wales, PA 19454, NDC… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval. |
| Initiation date | Mar 3, 2014 |
| Report date | Mar 26, 2014 |
| Termination date | Aug 14, 2014 |
| City | Concord |
| State | NC |
| Country | United States |
| FEI number | 3000206187 |
At a glance
- 1–9 Products in this recall
- 1–9 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: