Severity
Low
FDA Food recall · Reported March 22, 2023
Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.
Mason Vitamins, Inc. recalled People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement - a low-severity action.
People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement was recalled by Mason Vitamins, Inc. in March 22, 2023. Reason: Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.. Check the official notice for the remedy. Verify recall #F-0424-2023 with the FDA Food before acting.
The recall
Mason Vitamins, Inc. issued this low-severity FDA Food recall-Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims..
Sourced from official FDA Food enforcement records. Verify recall #F-0424-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0424-2023) was formally reported on March 22, 2023, with the manufacturer initiating the action on November 14, 2022. It is classified under Low severity (Class III), with a current status of Terminated. Mason Vitamins, Inc. is listed as the recalling firm, operating out of Miami Lakes, FL. Federal records list the affected scope as 224,279 bottles.
The documented reason for this recall is: Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims. Distribution data in the federal record shows the product reached: Domestic distribution only.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
224,279 bottles
Related Recalls
6
6 from same agency
People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement
Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0424-2023 |
| Date reported | March 22, 2023 |
| Date initiated | November 14, 2022 |
| Recalling firm | Mason Vitamins, Inc. |
| Firm location | Miami Lakes, FL |
| Affected scope | 224,279 bottles |
| Distribution | Domestic distribution only. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
Pure Vitamins and Natural Supplements, LLC · 2026-04-15
Pure Vitamins and Natural Supplements, LLC · 2026-04-15
Herbal Creations USA · 2026-04-01
Winder Laboratories, LLC · 2026-03-25
Imu-Tek Animal Health, Incorporated · 2026-02-11
Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 22, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.