Recall company profile

Pharmavite Corporation Recalls

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

4recall records
Nov 27, 2013latest record date
Nov 27, 2013earliest record date

Recall history in this database

Classification mix: Class II: 4.

FoodNov 27, 2013

Pharmavite Multi for Her 50+ recall — FDA F-0186-2014

Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her,…

Class IIFDA: TerminatedPharmavite Corporation
FoodNov 27, 2013

Pharmavite Multi for Her recall — FDA F-0185-2014

Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her,…

Class IIFDA: TerminatedPharmavite Corporation
FoodNov 27, 2013

Pharmavite Multi For Him recall — FDA F-0187-2014

Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her,…

Class IIFDA: TerminatedPharmavite Corporation
FoodNov 27, 2013

Pharmavite Multi Complete recall — FDA F-0184-2014

Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her,…

Class IIFDA: TerminatedPharmavite Corporation

Understanding this recall history

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