Class I · High risk
Rugby brand Lubricating Tears Eye Drops
Non-Sterility
Up&Up brand dry eye relief
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Non-Sterility
Cause type: Sterility / contamination
A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.
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
Affected NDC
76168-0800-30
Compare with the code on your package — it is the most precise check available.
- Recalling firm
- Kilitch Healthcare India Limited
- NDC code
- 76168-800-30
- Origin
- India
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0311-2024 · FDA notice
Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week.
Other recalls by Kilitch Healthcare India Limited
All 2023 recalls
Class I · High risk
Lubricant Eye Drops
Non-Sterility
Class I · High risk
Multi-action Relief Drops
Non-Sterility
Class I · High risk
Lubricant Gel Drops
Non-Sterility
Other sterility / contamination recalls from 2023
All sterility / contamination recalls
Class II · Moderate risk
DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose
Lack of Sterility Assurance
Class II · Moderate risk
ceFAZolin sodium in Sterile Water for injection
Lack of assurance of sterility.
Class I · High risk
Rugby brand Lubricating Tears Eye Drops
Non-Sterility
Class I · High risk
Lubricant Eye Drops
Non-Sterility
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