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Class II: temporary or reversible health riskTerminated

Medtech Products SUCRETS Sore Throat & Cough Vapor Cherry Recall

SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist

Medtech Products, Inc. · Tarrytown, NY

Risk level
Class II
Reported by FDA
Jun 10, 2015
Recall ID
D-1113-2015
Check your lot numberHow we source this data

Summary

Medtech Products recalled SUCRETS Sore Throat & Cough Vapor Cherry starting May 21, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1113-2015 on Jun 10, 2015. Reason: Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat, Cough & Dry Mouth Honey Lemon lozenges was applied to the underside of the Sucrets Sore Throat & Cough Vapor Cherry lozenges tin. Status: Terminated.

Why it was recalled

Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat, Cough & Dry Mouth Honey Lemon lozenges was applied to the underside of the Sucrets Sore Throat & Cough Vapor Cherry lozenges tin.

Product description

SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433

Lot numbers, UPCs & expiration codes

Lot #: 42451, Exp 09/17

Where it was sold

Nationwide and Puerto Rico

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-1113-2015
Classification
Class II
Status
Terminated
Recall initiated
May 21, 2015
FDA report date
Jun 10, 2015
Quantity
107,832 tins
Recall type
Voluntary: Firm initiated
Recalling firm
Medtech Products, Inc.

Original FDA data

Every field from FDA enforcement report D-1113-2015, exactly as published.

Show all FDA fields
City
Tarrytown
State
NY
Status
Terminated
Country
United States
Event ID
71319
Address
660 White Plains Rd
Code information
Lot #: 42451, Exp 09/17
Postal code
10591-5139
Report date
Jun 10, 2015
Product type
Drugs
Recall number
D-1113-2015
Classification
Class II
Recalling firm
Medtech Products, Inc.
Product quantity
107,832 tins
Termination date
Jun 6, 2018
Reason for recall
Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat, Cough & Dry Mouth Honey Lemon lozenges was applied to the underside of the Sucrets Sore Throat & Cough Vapor Cherry lozenges tin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
May 21, 2015
Initial firm notification
Letter
Center classification date
Jun 1, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1113-2015, published Jun 10, 2015. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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