CLASS III Food recall · Reported 22 Mar 2023 · FDA Enforcement Report
People's Choice Women's Daily Vitamins with Iron, Dietary Supplement recalled
Mason Vitamins is recalling People's Choice Women's Daily Vitamins with Iron, Dietary Supplement. The recall was initiated on 14 Nov 2022 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0424-2023
- FDA event ID
- 91155
- Recalling firm
- Mason Vitamins, Miami Lakes, FL
- Brand
- People's Choice
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 14 Nov 2022
- FDA classified
- 10 Mar 2023
- Reported
- 22 Mar 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Vitamins
Timeline
| 14 Nov 2022 | Recall initiated by company | |
| 10 Mar 2023 | Classified by FDA | +116 days |
| 22 Mar 2023 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.
Product as listed by the FDA
People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement
Where it was distributed
Domestic distribution only.
Questions about this recall
Why was it recalled?
Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.
Which lots are affected?
Lot No./Expiration Date o 25807G/9-24 o A25807G/9-24 o B25807G/9-24 o C25807G/9-24 o D25807G/9-24
Where was it sold?
Domestic distribution only.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 91155| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS III | Healthy Sense Daily Multiple with Iron, Dietary Supplement recalledHealthy Sense | Mason Vitamins | Other | FL |
More recalls from Mason Vitamins
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS III | Healthy Sense Daily Multiple with Iron, Dietary Supplement recalledHealthy Sense | Mason Vitamins | Other | FL |
| Food | CLASS III | Coenzyme Q-10 50 mg label reads in part recalled by Mason VitaminsCoenzyme | Mason Vitamins | Labeling Errors | 31 states |
Other Vitamins recalls
All 294| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | FulviLife Complex recalled by Wellnov SupplementsFulviLife Complex | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid recalledLiposomal D3-5000IU | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Joint Nourish recalled by Wellnov SupplementsJoint Nourish | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal Mens Liquid Multivitamin Drops recalled by Wellnov SupplementsLiposomal Mens | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal Womens 50+ Liquid Multivitamin Drops recalledLiposomal Womens | Wellnov Supplements | Botulism | Nationwide |