FDAFDA · Food and drugs·Recall number D-0667-2017
Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
Published April 19, 2017 · Recall initiated: March 16, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LUMIGAN
- Manufacturer
- Allergan Sales, LLC
- Distributor
- Nationwide in the US
- Lot
- Lot #: 92577, Exp. JUN 2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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