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Class II: temporary or reversible health riskTerminated

Medtech Products Clear Eyes Assorted Sidekick Floor Stand Recall

Clear Eyes Assorted Sidekick Floor Stand Display

Medtech Products, Inc. · Tarrytown, NY

Risk level
Class II
Reported by FDA
Aug 28, 2019
Recall ID
D-1828-2019
Check your lot numberHow we source this data

Summary

Medtech Products recalled Clear Eyes Assorted Sidekick Floor Stand starting Jul 26, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1828-2019 on Aug 28, 2019. Reason: 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. Status: Terminated.

Why it was 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.

Product description

Clear Eyes Assorted Sidekick Floor Stand Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye drops, 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline hydrochloride 0.03%), 0.5 FL OZ (15 mL) bottle (UPC 6 78112 66577 8); and c) Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%), 0.5 FL OZ (15 mL) bottle (UPC 6 78112 65920 3); Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, case UPC 00678112106905.

Lot numbers, UPCs & expiration codes

Lot #: Display 17E12A, Exp 09/19; lot and expiry for individual products within this display are captured in each individual product Code Information

Where it was sold

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

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-1828-2019
Classification
Class II
Status
Terminated
Recall initiated
Jul 26, 2019
FDA report date
Aug 28, 2019
Quantity
25,992 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Medtech Products, Inc.

Original FDA data

Every field from FDA enforcement report D-1828-2019, exactly as published.

Show all FDA fields
City
Tarrytown
State
NY
Status
Terminated
Country
United States
Event ID
83417
Address
660 White Plains Rd Ste 250
Code information
Lot #: Display 17E12A, Exp 09/19; lot and expiry for individual products within this display are captured in each individual product Code Information
Postal code
10591-5171
Report date
Aug 28, 2019
Product type
Drugs
Recall number
D-1828-2019
Classification
Class II
Recalling firm
Medtech Products, Inc.
Product quantity
25,992 bottles
Termination date
Mar 10, 2021
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Clear Eyes Assorted Sidekick Floor Stand Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye drops, 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline hydrochloride 0.03%), 0.5 FL OZ (15 mL) bottle (UPC 6 78112 66577 8); and c) Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%), 0.5 FL OZ (15 mL) bottle (UPC 6 78112 65920 3); Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, case UPC 00678112106905.
Distribution pattern
Nationwide in the USA and Puerto Rico, St. Michael, Barbados, Guyana, St. Johns, Antigua and Barbuda, Kingston 5, and Jamaica.
Recall initiation date
Jul 26, 2019
Initial firm notification
Letter
Center classification date
Aug 16, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1828-2019, published Aug 28, 2019. View the source record (openFDA) · FDA enforcement reports

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

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