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Class II · ModerateActive recall

Gentle Eyes Lubricant Eye Drops

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # 3279, Exp 6/30/2027; Lot # 3292, Exp 5/31/2027.
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Lack of Assurance of Sterility

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byTRP Company
Brand nameGENTLE EYES LUBRICANT EYE DROPS
Generic nameCARBOXYMETHYLCELLULOSE SODIUM
Active ingredient(s)CARBOXYMETHYLCELLULOSE SODIUM
Distributed by / forSterling Pharmaceutical Services LLC
NDC17312-430-15
Show the full FDA record
Full product labelTRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci Ln, Reno, NV 89502, NDC 17312-430-15.
Recalling firmSterling Pharmaceutical Services LLC
DistributionUSA Nationwide
Quantity14538 bottles
Recall initiated2026-08-20
Report date2026-09-30
Recall completed—
Recall numberD-0860-2026
ClassificationClass II
FDA statusOngoing
Origin on fileDupo IL United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.