ActivEyes Altachlore Solution recall: Sterility Concern
ActivEyes Altachlore Solution, 15 mL (1/2 FL OZ), Manufactured by Altaire Pharmaceuticals Inc., Aquebogue, NY 11931, NDC 59390-183-13
Why was ActivEyes Altachlore Solution recalled?
Lack of Assurance of Sterility
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
18008 1/20 8/13/2018 19050 2/22 3/18/2019 19105 4/22
- Product
- ActivEyes Altachlore Solution, 15 mL (1/2 FL OZ), Manufactured by Altaire Pharmaceuticals Inc., Aquebogue, NY 11931, NDC 59390-183-13
- Recalling firm
- Altaire Pharmaceuticals, Inc.
- Quantity
- 22494 units
- Distribution
- U.S.A. Nationwide
- Recall date
- November 27, 2019
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)