PReye Vitamin See Eye Drops Recall: Lack of Sterility Assurance
PReye Vitamin See Antioxidant Preservative Free Eye Drops recalled due to lack of sterility assurance. All lots within expiry date are affected.
Recall notice
Lack of Assurance of Sterility
Contact the company
What happened, in plain English
PReye Vitamin See Antioxidant Preservative Free Eye Drops are being recalled because they may not be sterile. This could lead to eye infections if used. Read more at govinfonow.com/recall/31302-preye-vitamin-see-eye-drops-recall-lack-of-sterility-assurance.
Source Summary by GovInfoNow · govinfonow.com/recall/31302-preye-vitamin-see-eye-drops-recall-lack-of-sterility-assurance · Updated August 17, 2026 · FDA enforcement record: FDA #D-0621-2026
Cite this page
“PReye Vitamin See Eye Drops Recall: Lack of Sterility Assurance.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31302-preye-vitamin-see-eye-drops-recall-lack-of-sterility-assurance. Based on FDA recall #D-0621-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0621-2026%22&limit=1).
Why it’s dangerous
The eye drops may not be sterile, which can cause infections. This is a serious health risk, especially for individuals with weakened immune systems.
Who’s affected
People who own or use PReye Vitamin See Antioxidant Preservative Free Eye Drops. Those with compromised immune systems are at higher risk.
How to tell if you have this one
Check for PReye Vitamin See Antioxidant Preservative Free Eye Drops. All lots within expiry date are affected.
- Brand
PReye- Category
Drug
What to do — step by step
Check Product
Look for PReye Vitamin See Antioxidant Preservative Free Eye Drops with any expiry date.
Where it went and when
Where it was distributed
Distributed in Colorado.
FDA distribution: “CO” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado.
Recall timeline
FDA published this recall 44 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0621-2026 (May 18, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0621-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.