CLASS II ONGOING Drug recall · Reported 1 Jul 2026 · FDA Enforcement Report

Vitamin See Antioxidant Preservative Free Eye Drops recalled by PReye

PReye is recalling Vitamin See Antioxidant Preservative Free Eye Drops, distributed in Colorado. The recall was initiated on 18 May 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots within expiry
Quantity recalledapproximate 50 to 60 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-0621-2026
FDA event ID
99032
Recalling firm
PReye, Wheat Ridge, CO
Classification
Class II
Status
Ongoing
Recall initiated
18 May 2026
FDA classified
24 Jun 2026
Reported
1 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
N/A
Reason category
Sterility
Drug class
Eye Drops

Timeline

18 May 2026Recall initiated by company
24 Jun 2026Classified by FDA+37 days
1 Jul 2026Published in enforcement report+7 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

PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, CO

Where it was distributed

CO

Colorado

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

All lots within expiry

Where was it sold?

CO

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.