Myson Corporation, Inc. Recalls

Overview of recall records associated with Myson Corporation, Inc., including dates, categories and classifications where available.

2recall records

Dec 18, 2013latest record date

Dec 18, 2013earliest record date

Recall history in this database

Classification mix: Class I: 2.

DrugDec 18, 2013

Myson Corporation Volcano Male Enhancement 1500mg, 1-count capsule recall — FDA D-345-2014

Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and Volcano Capsules, marketed as dietary supplements, are being recalled because they were found to contain undeclared…

Class IFDA: TerminatedMyson Corporation, Inc.

DrugDec 18, 2013

Myson Corporation Volcano Male Enhancement Liquid, 2 FL OZ (60 ml) bottle recall — FDA D-344-2014

Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and Volcano Capsules, marketed as dietary supplements, are being recalled because they were found to contain undeclared…

Class IFDA: TerminatedMyson Corporation, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Myson Corporation, 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.