US Drug Recall Register
Class II · Moderate risk Completed Initiated Feb 23, 2017 (10 years ago)

Aspirin Chewable Tablets, 81 mg, (NSAID*), packaged in UD 750 Tablets (25 x 30) tablets…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance: foreign material found in the bulk inventory.

What was recalled

Aspirin Chewable Tablets, 81 mg, (NSAID*), packaged in UD 750 Tablets (25 x 30) tablets in blisters per carton, Dist. By: McKesson Packaging Services, a business unit of McKesson Corporation, 7101 Weddington Rd., Concord, NC 28027, NDC 63739-434-01.

Recalling firm
Mckesson Packaging Services
NDC code
63739-434-01
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0513-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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