PReye Vitamin See Eye Drops Recall Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
PReye LLC is recalling approximately 50-60 bottles of PReye Vitamin See Antioxidant Preservative Free Eye Drops in Colorado due to lack of assurance of sterility.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 3, 2026 and geographically references Colorado. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened
PReye LLC has initiated a voluntary recall of PReye Vitamin See Antioxidant Preservative Free Eye Drops due to lack of assurance of sterility. The recall is classified as Class II.
Which Products Are Affected
The affected product is PReye Vitamin See Antioxidant Preservative Free Eye Drops, distributed by PReye, LLC, Golden, CO. Approximately 50 to 60 bottles are involved, covering all lots within expiry. Distribution was limited to CO.
What You Should Do
The recall was initiated voluntarily by the firm. Consumers should verify product details against the FDA recall information.
Why This Matters
The recall addresses potential sterility concerns for eye drops distributed in Colorado.
Source
FDA recall number D-0621-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (761 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 3, 2026.
Frequently Asked Questions
Common questions about this FDA recall.