Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Ongoing Initiated Nov 13, 2023 (3 years ago)

Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium)

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

Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%), packaged in 0.5 FL OZ (15 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0089-1

Affected NDC 70000-0089-01

Compare with the code on your package — it is the most precise check available.

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Dry Eye Relief
Carboxymethylcellulose sodium
NDC 70000-0089
, UNSPECIFIED 10 mg/mL Gel
Ophthalmic
Cardinal Health 110, LLC. Dba Leader OTC
Recalling firm
Kilitch Healthcare India Limited
NDC code
70000-0089-1
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0299-2024 · 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

Other sterility / contamination recalls from 2023

All sterility / contamination recalls