SUN PHARMACEUTICAL INDUSTRIES INC recalls Tretinoin Cream USP
- Recalling company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Product
- Tretinoin Cream USP, 0.05%, 45g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals USA Inc., Hawthorne, NY 10532, NDC 51672-1394-9.
- Reason
- Failed Impurities/Degradation Specifications
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Sep 25, 2026
- Reported
- Oct 14, 2026
- Distribution
- US Nationwide.
- Status
- Ongoing
- Quantity
- N/A
- Lot / codes
- Lot # AD96184, Exp Date: 12/31/2026.
- Company location
- Princeton, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0033-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0033-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.