# FDA recall D-0148-2017

> **Sun Pharmaceutical Industries, Inc.** · Class III · drug recall initiated 2016-10-28.

## Product

KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Sample: Not For Sale, Rx only, RANBAXY, Jacksonville, FL  32257, UPC 3 10631 09335 8.

## Reason for recall

Failed Stability Specifications: Low Out of Specification results for alcohol content.

## Distribution

NJ and further distributed Nationwide in the USA.

## Key facts

- **Recall number:** D-0148-2017
- **Recalling firm:** Sun Pharmaceutical Industries, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-28
- **Report date:** 2016-11-30
- **Termination date:** 2017-10-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0148-2017

## Citation

> AI Analytics. FDA recall D-0148-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0148-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*