Food recall: People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement
Class III FDA enforcement event 91155. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.
Class III, in the words of FDA
a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences
Mason Vitamins, Inc. started this food recall on 14 Nov 2022. The firm address in the FDA record is in Miami Lakes, FL. FDA put the recall in Class III. FDA event 91155 has 2 product records. The first FDA enforcement report date is 22 Mar 2023. The record gives the status Terminated, with the termination date 30 Nov 2023.
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.
Domestic distribution only.
Recalling firm
Mason Vitamins, Inc., Miami Lakes, FL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0424-2023 | People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement | 224,279 bottles | Class III | Terminated | 22 Mar 2023 |
| F-0425-2023 | Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets | 37,330 bottles/ 20 tablets ea | Class III | Terminated | 22 Mar 2023 |
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 III: The lowest of the three FDA recall classes.
The event in context
- Food events that started in 2022
- 452
- Share of these events in Class III
- 7%
- Product records in this event
- 2Median of the firm: 2
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 6 Jul 2015 | Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENER Event 71790 | Food | Class III | 1 |
Official channels
- FDA enforcement report F-0424-2023The 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.
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Cite this page
Recall Register. FDA enforcement event 91155. https://recallregister.com/fda/iii/91155/. 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:
Domestic distribution only.
- What quantity of product is in FDA event 91155?
- The event has 2 product records. The first record gives this quantity:
224,279 bottles
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2022 have the same class?
- 7% of the 452 food events that started in 2022 are in Class III.