FDAFDA · Food and drugs·Recall number D-927-2014
ASPIRIN, CHEW Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536329736.
Published January 29, 2014 · Recall initiated: July 2, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Label Mixup: ASPIRIN, CHEW Tablet, 81 mg may have potentially been mislabeled as one of the following drugs: OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: AD30028_4, EXP: 5/8/2014; MODAFINIL, Tablet, 200 mg, NDC 00603466216, Pedigree: W002760, EXP: 6/6/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W003015, EXP: 6/12/2014; VITAMIN B COMPLEX
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Aidapak Services, LLC
- Distributor
- Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
- Lot
- ASPIRIN, CHEW Tablet, 81 mg has the following codes: Pedigree: AD33897_1, EXP: 5/9/2014; Pedigree: W002773, EXP: 6/6/2014; Pedigree: W003093, EXP: 6/13/2014; Pedigree: W003459, EXP: 6/20/2014; Pedigree: AD49582_1, EXP: 5/16/2014.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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