FDAClass IINovember 27, 2019

Natural Ophthalmics Ortho-K Thin Eye Drops recall: Sterility Concern

Natural Ophthalmics Ortho-K Thin Eye Drops, 15 mL, NDC 68770-144-15

Why was Natural Ophthalmics Ortho-K Thin Eye Drops 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?

17375 12/19 17376 12/19 18190 7/20 18191 8/20

Product
Natural Ophthalmics Ortho-K Thin Eye Drops, 15 mL, NDC 68770-144-15
Recalling firm
Altaire Pharmaceuticals, Inc.
Quantity
84216 units
Distribution
U.S.A. Nationwide
Recall date
November 27, 2019
Classification
Class II
Status
Completed
Agency
FDA (drug)
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