Food recall: vitafusion MultiVites 150ct,
Class II FDA enforcement event 87745. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Potential presence of a metallic mesh material in products.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Church & Dwight Co., Inc. OGI Distribution Center started this food recall on 19 Apr 2021. The firm address in the FDA record is in North Brunswick, NJ. FDA put the recall in Class II. FDA event 87745 has 6 product records. The first FDA enforcement report date is 5 May 2021. The record gives the status Terminated, with the termination date 3 Feb 2022.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
The product was distributed thru out the US and Canada, Panama, China,
Recalling firm
Church & Dwight Co., Inc. OGI Distribution Center, North Brunswick, NJ.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
6 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0461-2021 | vitafusion MultiVites 150ct, | 683 Bottles | Class II | Terminated | 5 May 2021 |
| F-0462-2021 | vitafusion Fiber Well 220ct, 10 / 220 CT | 2928 Bottles | Class II | Terminated | 5 May 2021 |
| F-0463-2021 | vitafusion Fiber Well 90ct, 4/3 Pack 90CT | 7782 Bottles | Class II | Terminated | 5 May 2021 |
| F-0464-2021 | vitafusion Melatonin 140ct, 3 Pack 140 CT vitafusion Melatonin 44ct , 3Pack 44CT | 5475 Bottles 44ct Bottles, 2081 Bottles 140 CT | Class II | Terminated | 5 May 2021 |
| F-0465-2021 | vitafusion Kids Melatonin 50ct, 4 / 3 PACK 50CT | 1320 Bottles | Class II | Terminated | 5 May 2021 |
| F-0466-2021 | vitafusion SleepWell 250ct / 24 / 250 CT | 120 Bottles | Class II | Terminated | 5 May 2021 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2021
- 463
- Share of these events in Class II
- 57%
- Product records in this event
- 6
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-0461-2021The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 87745. https://recallregister.com/fda/ii/87745/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
The product was distributed thru out the US and Canada, Panama, China,
- What quantity of product is in FDA event 87745?
- The event has 6 product records. The first record gives this quantity:
683 Bottles
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2021 have the same class?
- 57% of the 463 food events that started in 2021 are in Class II.