# FDA recall D-780-2014

> **Aidapak Services, LLC** · Class II · drug recall initiated 2013-07-02.

## Product

TOLTERODINE TARTRATE ER, Capsule, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00009519001.

## Reason for recall

Labeling: Label Mixup: TOLTERODINE TARTRATE ER, Capsule, 2 mg may be potentially mislabeled as one of the following drugs:  RANOLAZINE ER	, Tablet, 500 mg, NDC 61958100301, Pedigree: AD62995_7, EXP: 5/29/2014;  FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe), NDC 00904759160, Pedigree: W002717, EXP: 6/6/2014.

## Distribution

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

## Key facts

- **Recall number:** D-780-2014
- **Recalling firm:** Aidapak Services, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-02
- **Report date:** 2014-01-29
- **Termination date:** 2014-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vancouver, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-780-2014

## Citation

> AI Analytics. FDA recall D-780-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-780-2014. Source: US FDA. Licensed CC0.

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