# FDA recall D-1285-2015

> **Actavis Laboratories, FL, Inc.** · Class III · drug recall initiated 2015-06-23.

## Product

Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by Actavis Pharma, Inc. Parsippany, NJ 07054 USA.  NDC: 0591-2464-01.

## Reason for recall

Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.

## Distribution

U.S. Nationwide including Puerto Rico.

## Key facts

- **Recall number:** D-1285-2015
- **Recalling firm:** Actavis Laboratories, FL, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-23
- **Report date:** 2015-08-12
- **Termination date:** 2016-12-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Davie, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1285-2015

## Citation

> AI Analytics. FDA recall D-1285-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1285-2015. Source: US FDA. Licensed CC0.

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