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Class II: temporary or reversible health riskTerminated

Ultra Seal Backache & Muscle Relief Recall

Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg…

Ultra Seal Corporation · New Paltz, NY

Risk level
Class II
Reported by FDA
Feb 9, 2022
Recall ID
D-0482-2022
Check your lot numberHow we source this data

Summary

Ultra Seal recalled Backache & Muscle Relief starting Jan 24, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0482-2022 on Feb 9, 2022. Reason: cGMP deviations. Status: Terminated.

Why it was recalled

cGMP deviations

Product description

Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-111-832

Lot numbers, UPCs & expiration codes

Lot #: K9770, AK9770 Exp. Date 08/2022; AK9958, K9958 Exp. Date 12/2022; AK9717, Exp. Date 07/2022; AK9522, AK9641 , Exp. Date 03/2022; AK9817, Exp. Date 09/2022

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-0482-2022
Classification
Class II
Status
Terminated
Recall initiated
Jan 24, 2022
FDA report date
Feb 9, 2022
Quantity
5,107,565 packets
Recall type
Voluntary: Firm initiated
Recalling firm
Ultra Seal Corporation

Original FDA data

Every field from FDA enforcement report D-0482-2022, 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 #: K9770, AK9770 Exp. Date 08/2022; AK9958, K9958 Exp. Date 12/2022; AK9717, Exp. Date 07/2022; AK9522, AK9641 , Exp. Date 03/2022; AK9817, Exp. Date 09/2022
Postal code
12561-1609
Report date
Feb 9, 2022
Product type
Drugs
Recall number
D-0482-2022
Classification
Class II
Recalling firm
Ultra Seal Corporation
Product quantity
5,107,565 packets
Termination date
Oct 16, 2023
Reason for recall
cGMP deviations
Voluntary / mandated
Voluntary: Firm initiated
Product description
Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-111-832
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-0482-2022, 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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