Severity
Moderate
CPSC recall on September 24, 2020. Classified as Moderate severity. Approximately About 8,200 units are affected. The recall was issued because: The multivitamins' packaging is not child resistant as required by the Poison Prevention Packaging Act. The capsules in…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This CPSC action (record #20782) was formally reported on September 24, 2020. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records indicate About 8,200 units are affected.
The documented reason for this recall is: The multivitamins' packaging is not child resistant as required by the Poison Prevention Packaging Act. The capsules inside the bottle contain iron, which can cause serious injury or death to young children if multiple … Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately store the product in a safe location out of reach of children. Contact The Vitamin Shoppe for instructions on how to dispose of the product and receive a full refund or m… — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 1 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 6 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
About 8,200
Related Recalls
6
1 from same agency
This recall involves The Vitamin Shoppe's Vthrive Bioactive Women's One-Daily Multi vitamins. The 60-count capsules were sold in an amber bottle with a gray top. Vthrive and Bioactive Women's One-Daily Multi are printed on a blue label on the bottle. Item number VS-6104 can be found on the back of the bottle and lot number 006218, 006454, 006495 or 006779 on the bottle's underside. Only the 60-count bottles are included in this recall.
The multivitamins' packaging is not child resistant as required by the Poison Prevention Packaging Act. The capsules inside the bottle contain iron, which can cause serious injury or death to young children if multiple tablets are ingested at once.
Consumers should immediately store the product in a safe location out of reach of children. Contact The Vitamin Shoppe for instructions on how to dispose of the product and receive a full refund or merchandise credit. The Vitamin Shoppe is notifying all known purchasers directly.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 20782 |
| Date reported | September 24, 2020 |
| Date initiated | September 24, 2020 |
| Recalling firm | Not disclosed |
| Units affected | About 8,200 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
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Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).