Multiple brands: Lubricant Eye Drops & Multi-Symptom Eye Drops — FDA announcement Jan 22, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Jan 22, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Lubricant Eye Drops & Multi-Symptom Eye Drops
Reason
Device & Drug Safety Potential Safety Concerns
Classification
Not supplied
Recalling firm
Kilitch Healthcare India Limited
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
b77aa96ebe3f684a

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityProduct | Product Information | NDC NO (wrongly Mention is last press release) | NDC Nos (Corrected, to be read as) | Retailer / Label; LUBRICANT GEL DROPS 15 ML | Carboxymethylcellulose Sodium Eye Drops 1.0% W/V | 11822-9706-5 | 11822-4540-5 | Rite Aid; LUBRICANT EYE DROPS 15ML (TWIN PACK) | Carboxymethylcellulose Sodium Eye Drops 0.5% W/V | 11822-9707-5 | 11822-4811-5 | Rite Aid

Match all identifying details in the current notice. A brand name alone is not enough.

Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

FDA company announcement, table 1
Product Product Information NDC NO (wrongly Mention is last press release) NDC Nos (Corrected, to be read as) Retailer / Label
LUBRICANT GEL DROPS 15 ML Carboxymethylcellulose Sodium Eye Drops 1.0% W/V 11822-9706-5 11822-4540-5 Rite Aid
LUBRICANT EYE DROPS 15ML (TWIN PACK) Carboxymethylcellulose Sodium Eye Drops 0.5% W/V 11822-9707-5 11822-4811-5 Rite Aid

Announcement retrieved Oct 1, 2026. Official announcement.

Distribution

These products were distributed nationwide to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Jan 22, 2024
Company announcement date
Jan 19, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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