Allergan Sales, LLC recalls Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
- Recall date
- March 16, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0667-2017
- FDA classification
- Class III
- Brand / firm
- Allergan Sales, LLC
- Sold / distributed
- Nationwide in the US
Why it was recalled
Failed Impurities/Degradation Specifications
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
Get recall alerts
Free email alert whenever Allergan Sales, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Allergan Sales, LLC