Data Foundry

Drug recalls 2019

Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display — Class II drug recall D-1833-2019

Terminated recall by Medtech Products, Inc., reported 2019-08-28, distributed nationwide. CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the

Recall numberD-1833-2019
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedtech Products, Inc., Tarrytown, NY, United States
Recall initiated2019-07-26
Classified2019-08-16
Reported by FDA2019-08-28
Terminated2021-03-10
DistributedNationwide (US)
Countries outside the USBB, GY, JM
Quantity793,872 bottles
Reason classescgmp
UPC / GTIN / UDI-DI00678112254187, 30300742541283
Lot numbers02/20, 04/20, 09/19, 10/19, 16242, 16280, 17051, 17130

Product

Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display; each display (case UPC 30300742541283) contains 48 each of Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed by Medtech Products Inc., Tarrytown, NY 10591; A Prestige Brands Company.

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1833-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.