CLASS II Drug recall · Reported 28 Aug 2019 · FDA Enforcement Report

Clear Eyes Redness Relief Display recalled by Medtech Products

Medtech Products is recalling Clear Eyes Redness Relief Display, distributed nationwide in the US. The recall was initiated on 26 Jul 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 3-pack Q16299D2, Exp 07/19; Q162300D1, Q16260B1, Q16261B1, Q16263B1, Q16301D1, Q16302D1, Q16303D1, Q16308D1, Q16309D1, Q16336D1, Q16337D1, Q16340D1, Q16342D1, Q16343D1, Q16344D1, Exp 08/19; lot and expiry for individual products within this display are captured in each individual product Code Information
Quantity recalled124,038 bottles

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-1829-2019
FDA event ID
83417
Recalling firm
Medtech Products, Tarrytown, NY
Classification
Class II
Status
Terminated
Recall initiated
26 Jul 2019
FDA classified
16 Aug 2019
Reported
28 Aug 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Eye Drops

Timeline

26 Jul 2019Recall initiated by company
16 Aug 2019Classified by FDA+21 days
28 Aug 2019Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.

Product as listed by the FDA

Clear Eyes Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10552 6) of Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye drops, 0.5 FL OZ (15 mL) bottle (individual bottle UPC 6 78112 25415 6); Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company.

Where it was distributed

Nationwide in the USA and Puerto Rico, St. Michael, Barbados, Guyana, St. Johns, Antigua and Barbuda, Kingston 5, and Jamaica.

Nationwide Puerto Rico

Questions about this recall

Is Clear Eyes Redness Relief Display recalled?

Yes. Medtech Products recalled Clear Eyes Redness Relief Display on 26 Jul 2019. The recall is Class II and its status is Terminated. Recall number D-1829-2019.

Why was it recalled?

CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.

Which lots are affected?

Lot #: 3-pack Q16299D2, Exp 07/19; Q162300D1, Q16260B1, Q16261B1, Q16263B1, Q16301D1, Q16302D1, Q16303D1, Q16308D1, Q16309D1, Q16336D1, Q16337D1, Q16340D1, Q16342D1, Q16343D1, Q16344D1, Exp 08/19; lot and expiry for individual products within this display are captured in each individual product Code Information

Where was it sold?

Nationwide in the USA and Puerto Rico, St. Michael, Barbados, Guyana, St. Johns, Antigua and Barbuda, Kingston 5, and Jamaica.

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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Medtech Products

All 18