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Class II: temporary or reversible health riskOngoing

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare Clear Eyes Redness Relief Recall

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company · Tarrytown, NY

Risk level
Class II
Reported by FDA
Sep 30, 2026
Recall ID
D-0870-2026
Check your lot numberHow we source this data

Summary

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare recalled Clear Eyes Redness Relief starting Sep 15, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0870-2026 on Sep 30, 2026. Reason: Lack of Assurance of Sterility. Status: Ongoing.

Why it was recalled

Lack of Assurance of Sterility

Product description

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15

Lot numbers, UPCs & expiration codes

Lot #: RL25G02, RL25G03, RL25G04, Exp. Date Jul-27; RL25H02, RL25H03, RL25H04, Exp. Date Aug-27; RL25K01, RL25K02, RL25K03, RL25K04, Exp. Date Sep-27; RL25M01, RL25M02, RL25M03, RL25M04, Exp. Date Oct-27; RL25N01, RL25N02, RL25N04, Exp. Date Nov-27.

Where it was sold

Nationwide in the USA.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0870-2026
Classification
Class II
Status
Ongoing
Recall initiated
Sep 15, 2026
FDA report date
Sep 30, 2026
Quantity
2,356,248 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Original FDA data

Every field from FDA enforcement report D-0870-2026, exactly as published.

Show all FDA fields
City
Tarrytown
State
NY
Status
Ongoing
Country
United States
Event ID
99909
Address
660 White Plains Rd Ste 250
Code information
Lot #: RL25G02, RL25G03, RL25G04, Exp. Date Jul-27; RL25H02, RL25H03, RL25H04, Exp. Date Aug-27; RL25K01, RL25K02, RL25K03, RL25K04, Exp. Date Sep-27; RL25M01, RL25M02, RL25M03, RL25M04, Exp. Date Oct-27; RL25N01, RL25N02, RL25N04, Exp. Date Nov-27.
Postal code
10591-5171
Report date
Sep 30, 2026
Product type
Drugs
Recall number
D-0870-2026
Classification
Class II
Recalling firm
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
Product quantity
2,356,248 bottles
Reason for recall
Lack of Assurance of Sterility
Voluntary / mandated
Voluntary: Firm initiated
Product description
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
Distribution pattern
Nationwide in the USA.
Recall initiation date
Sep 15, 2026
Initial firm notification
Letter
Center classification date
Sep 23, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0870-2026, published Sep 30, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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