Class IITerminated in FDA datasetApr 19, 2021

vitafusion MultiVites 150ct

Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center

Why it was recalled

Potential presence of a metallic mesh material in products.

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Productvitafusion MultiVites 150ct,

FDA code information

Product Code: 027917019192 Lot Codes: WA03044959

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Full FDA record and distribution details

Original product description

vitafusion MultiVites 150ct,

Extracted codes and context

TypeCode / valueContext
lotWA03044959Product Code: 027917019192 Lot Codes: WA03044959

Recall details

Recall number
F-0461-2021
Event ID
87745
FDA status
Terminated
Initiated
Apr 19, 2021
Reported
May 5, 2021
Classified
Apr 28, 2021
Terminated
Feb 3, 2022
Quantity
683 Bottles
Location
North Brunswick, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

The product was distributed thru out the US and Canada, Panama, China,

FDA source record · F-0461-2021

Data updated September 16, 2026. View official FDA data ↗

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