CLASS II ONGOING Drug recall · Reported 30 Sep 2026 · FDA Enforcement Report

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops recalled

Sterling Pharmaceutical Services is recalling TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium, distributed nationwide in the US. The recall was initiated on 20 Aug 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 3279, Exp 6/30/2027; Lot # 3292, Exp 5/31/2027.
NDC17312-430
Quantity recalled14538 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0860-2026
FDA event ID
99712
Recalling firm
Sterling Pharmaceutical Services, Dupo, IL
Manufacturer
TRP Company
Classification
Class II
Status
Ongoing
Recall initiated
20 Aug 2026
FDA classified
21 Sep 2026
Reported
30 Sep 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Drug class
Eye Drops

Timeline

20 Aug 2026Recall initiated by company
21 Sep 2026Classified by FDA+32 days
30 Sep 2026Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

TRP 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.

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot # 3279, Exp 6/30/2027; Lot # 3292, Exp 5/31/2027.

Where was it sold?

USA Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 6 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

8 other products · FDA event 99712

More recalls from Sterling Pharmaceutical Services

All 9

Other Carboxymethylcellulose recalls

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