RecallRadar
ModerateReported July 1, 2026 (10 days ago)

PReye Vitamin See Antioxidant Preservative Free Eye Drops

Recalled by PReye LLC

Drug recall

PReye LLC

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

PReye LLC has recalled PReye Vitamin See Antioxidant Preservative Free Eye Drops, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on July 1, 2026 and was initiated on May 18, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers PReye Vitamin See Antioxidant Preservative Free Eye Drops, with approximately approximate 50 to 60 bottles affected. The company behind the recall is PReye LLC, based in Wheat Ridge, CO. The FDA describes the product as: “PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, CO”

Why was PReye Vitamin See Antioxidant Preservative Free Eye Drops recalled?

According to the FDA, the stated reason for the recall is: “Lack of Assurance of Sterility.” In plain terms, this recall relates to a sterility or contamination concern.

Sterile medicines, such as injectables and eye drops, must be completely free of microorganisms and stray particles. This recall means that sterility could not be assured or that contamination was found or suspected. Using a non-sterile product of this kind can cause infections, which is why these recalls are treated seriously.

What should you do?

If you think you may have bought PReye Vitamin See Antioxidant Preservative Free Eye Drops, compare it against the product description and identifying codes (All lots within expiry) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact PReye LLC or your local health authority.

About this recall

This recall was distributed in CO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
July 1, 2026
Recall started
May 18, 2026
Distributed in
CO
What was recalled
PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, CO
Why it was recalled (as stated by the FDA)
Lack of Assurance of Sterility
How to identify the affected product
All lots within expiry
Amount recalled
approximate 50 to 60 bottles

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was PReye Vitamin See Antioxidant Preservative Free Eye Drops recalled?+

According to the FDA: Lack of Assurance of Sterility

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have PReye Vitamin See Antioxidant Preservative Free Eye Drops?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0621-2026. Information last synced from the FDA on July 11, 2026.