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Regular Strength Pain Reliever (acetaminophen 110 mg, aspirin 162 mg, Caffeine 32.4 mg, Salicylam...

FDA Recall #D-0498-2022 — Class II — January 24, 2022

Recall #D-0498-2022 Date: January 24, 2022 Classification: Class II Status: Terminated

Product Description

Regular Strength Pain Reliever (acetaminophen 110 mg, aspirin 162 mg, Caffeine 32.4 mg, Salicylamide 152 mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-0113-00

Reason for Recall

cGMP deviations

Recalling Firm

Ultra Seal Corporation — New Paltz, NY

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

1,180,000 packets

Distribution

Nationwide within the United States

Code Information

Lot #: AK9450, Exp. Date 01/2022

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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