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.
Overview of recall records associated with Zee Medical Products Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
This page summarizes recall records in which the official source identifies Zee Medical Products Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.