CLASS II ONGOING Drug recall · Reported 30 Sep 2026 · FDA Enforcement Report
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare is recalling Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, distributed nationwide in the US. The recall was initiated on 15 Sep 2026 and the FDA has classified it as Class II.
Check your package
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-0871-2026
- FDA event ID
- 99909
- Recalling firm
- Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare, Tarrytown, NY
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 15 Sep 2026
- FDA classified
- 23 Sep 2026
- Reported
- 30 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Eye Drops
Timeline
| 15 Sep 2026 | Recall initiated by company | |
| 23 Sep 2026 | Classified by FDA | +8 days |
| 30 Sep 2026 | Published 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
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
Where it was distributed
Nationwide in the USA.
Questions about this recall
Why was it recalled?
Lack of Assurance of Sterility
Which lots are affected?
Lot #: RL25G04, Exp. Date 07/2027; RL2H02, Exp. Date 08/2027.
Where was it sold?
Nationwide in the USA.
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
1 other product · FDA event 99909| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Sterility | Nationwide |
More recalls from Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Sterility | Nationwide |
| Drug | CLASS I | TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Benzene | Nationwide |
| Drug | CLASS I | Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic recalledAmericaine | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Benzene | Nationwide |
Other Clear Eyes Redness Relief recalls
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Sterility | Nationwide |