# FDA recall D-1167-2014

> **McKesson Packaging Services** · Class III · drug recall initiated 2014-03-03.

## Product

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 63739-0512-10

## Reason for recall

Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1167-2014
- **Recalling firm:** McKesson Packaging Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-03-03
- **Report date:** 2014-03-26
- **Termination date:** 2014-08-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Concord, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1167-2014

## Citation

> AI Analytics. FDA recall D-1167-2014. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-1167-2014. Source: US FDA. Licensed CC0.

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