Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Travoprost Ophthalmic Solution Recalled by Mylan Pharmaceuticals Inc Due to Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mylan Pharmaceuticals Inc directly.
Affected Products
Travoprost Ophthalmic Solution, USP, 0.004%, 2.5 mL bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505, NDC 0378-9651-32.
Quantity: 20,112 bottles
Why Was This Recalled?
Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance impurities/degradation during routine stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mylan Pharmaceuticals Inc
Mylan Pharmaceuticals Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report