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Class II: temporary or reversible health riskTerminated

Ultra Seal COLD TERMINATOR decongestant/cold relief Recall

COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5

Ultra Seal Corporation · New Paltz, NY

Risk level
Class II
Reported by FDA
Feb 9, 2022
Recall ID
D-0487-2022
Check your lot numberHow we source this data

Summary

Ultra Seal recalled COLD TERMINATOR decongestant/cold relief starting Jan 24, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0487-2022 on Feb 9, 2022. Reason: cGMP deviations. Status: Terminated.

Why it was recalled

cGMP deviations

Product description

COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packets, Manufactured for: Tellus Medical Products, Carlsbad, CA 92011, NDC 69103-2556

Lot numbers, UPCs & expiration codes

Lot #: AK9587, Exp. Date 02/2022

Where it was sold

Nationwide within the United States

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-0487-2022
Classification
Class II
Status
Terminated
Recall initiated
Jan 24, 2022
FDA report date
Feb 9, 2022
Quantity
226,400 packets
Recall type
Voluntary: Firm initiated
Recalling firm
Ultra Seal Corporation

Original FDA data

Every field from FDA enforcement report D-0487-2022, exactly as published.

Show all FDA fields
City
New Paltz
State
NY
Status
Terminated
Country
United States
Event ID
89464
Address
521 Main St
Code information
Lot #: AK9587, Exp. Date 02/2022
Postal code
12561-1609
Report date
Feb 9, 2022
Product type
Drugs
Recall number
D-0487-2022
Classification
Class II
Recalling firm
Ultra Seal Corporation
Product quantity
226,400 packets
Termination date
Oct 16, 2023
Reason for recall
cGMP deviations
Voluntary / mandated
Voluntary: Firm initiated
Product description
COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packets, Manufactured for: Tellus Medical Products, Carlsbad, CA 92011, NDC 69103-2556
Distribution pattern
Nationwide within the United States
Recall initiation date
Jan 24, 2022
Initial firm notification
Letter
Center classification date
Jan 31, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0487-2022, published Feb 9, 2022. 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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