US Drug Recall Register
Class I · High risk Ongoing Initiated Nov 13, 2023 (3 years ago)

Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Non-Sterility

What was recalled

Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL) each bottles (Twin Pack), Distributed by: Target Corporation Minneapolis, MN 55403, NDC 76168-800-30

Recalling firm
Kilitch Healthcare India Limited
NDC code
76168-800-30
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0311-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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