FDA recall record

Zee Medical Products ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC recall — FDA D-0041-2015

Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.

Class IIclassification
D-0041-2015official record ID
Oct 29, 2014report date

Recall record at a glance

Official recordD-0041-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmZee Medical Products Inc.
Report dateOct 29, 2014
Recall initiation dateOct 7, 2014
Quantity43,752 boxes
LocationIrvine, CA, United States

Official product description

ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528

Why the product was recalled

Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.

Distribution information

Nationwide in US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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