Why it was recalled
Failed Impurities/Degradation Specifications
Product description
Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
Lot numbers, UPCs & expiration codes
Lot #: 92577, Exp. JUN 2018
Where it was sold
Nationwide in the US
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0667-2017
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Mar 16, 2017
- FDA report date
- Apr 19, 2017
- Quantity
- 56,878 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Allergan Sales, LLC
Original FDA data
Every field from FDA enforcement report D-0667-2017, exactly as published.
Show all FDA fields
- City
- Waco
- State
- TX
- Status
- Terminated
- Country
- United States
- Event ID
- 76748
- Address
- 8301 Mars Dr
- Code information
- Lot #: 92577, Exp. JUN 2018
- Postal code
- 76712-6578
- Report date
- Apr 19, 2017
- Product type
- Drugs
- Recall number
- D-0667-2017
- Classification
- Class III
- Recalling firm
- Allergan Sales, LLC
- Product quantity
- 56,878 bottles
- Termination date
- May 1, 2019
- Reason for recall
- Failed Impurities/Degradation Specifications
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
- Distribution pattern
- Nationwide in the US
- Recall initiation date
- Mar 16, 2017
- Initial firm notification
- Letter
- Center classification date
- Apr 12, 2017