TRP Blur Relief recall: Sterility Concern
TRP Blur Relief, 15 mL, NDC 17312-002-11
Why was TRP Blur Relief 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?
16256 09/19 17194 7/20
- Product
- TRP Blur Relief, 15 mL, NDC 17312-002-11
- Recalling firm
- Altaire Pharmaceuticals, Inc.
- Quantity
- 24144 units
- Distribution
- U.S.A. Nationwide
- Recall date
- November 27, 2019
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)