# FDA recall D-1361-2014

> **Greenstone Llc** · Class I · drug recall initiated 2014-03-06.

## Product

Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone LLC, Peapack, NJ  07977, NDC 59762-0182-2, UPC 3 59762-0182-2 9.

## Reason for recall

Presence of Foreign Tablets/Capsules: report of a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule was found in a bottle of Effexor XR (venlafaxine HCl) 150 mg capsules that was packaged in the same packaging campaign as the recalled lot

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1361-2014
- **Recalling firm:** Greenstone Llc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-03-06
- **Report date:** 2014-06-18
- **Termination date:** 2017-05-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Peapack, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1361-2014

## Citation

> AI Analytics. FDA recall D-1361-2014. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1361-2014. Source: US FDA. Licensed CC0.

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