Sun Pharmaceutical Industries, Inc. recalls KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Samp…
- Recall date
- October 28, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0148-2017
- FDA classification
- Class III
- Brand / firm
- Sun Pharmaceutical Industries, Inc.
- Sold / distributed
- NJ and further distributed Nationwide in the USA.
Why it was recalled
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
Get recall alerts
Free email alert whenever Sun Pharmaceutical Industries, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Sun Pharmaceutical Industries, Inc.