FDAClass IIAugust 17, 2022

Eye-stream recall: CGMP Deviations

Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.

Why was Eye-stream recalled?

CGMP Deviations: products were stored outside the drug label specifications.

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?

Part# 0065053004

Product
Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
Quantity
16 boxes
Distribution
Nationwide in the USA.
Recall date
August 17, 2022
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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