Severity
Moderate
ModerateActive
CPSC recall · Reported January 31, 2013
FoodState Recalls Bottles of MegaFood One Daily Supplements Due to Lack of Child-Resistant Packaging
The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement tablets inside the bottle contain iron, which can cause serious injury or d…
FoodState Inc., of Derry, N.h. recalled The recalled supplement bottles are brown glass bottles that contain MegaFood One Daily T… — a moderate-severity action.
FoodState Recalls Bottles of MegaFood One Daily Supplements Due to Lack of Child-Resistan… was recalled by FoodState Inc., of Derry, N.h. in January 31, 2013. Reason: The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement table…. Remedy: Consumers should immediately place bottles of this product out of reach of children and r…. Verify recall #13110 with the CPSC before acting.
The recall
FoodState Inc., of Derry, N.h. issued this moderate-severity CPSC recall — The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement table….
- Moderate
- severity level
- January 31, 2013
- reported
Sourced from official CPSC enforcement records. Verify recall #13110 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #13110) was formally reported on January 31, 2013. It is classified under Moderate severity, with a current status of Active. FoodState Inc., of Derry, N.h. is listed as the recalling firm. Federal records list the affected scope as About 7,400 units.
The documented reason for this recall is: The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement tablets inside the bottle contain iron, which can cause serious injury or death to young children if multiple table… 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 place bottles of this product out of reach of children and return any recalled bottles to the original place of purchase for a full refund or replacement. — consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls — 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.
Food recalls over time
Where this recall sits in its category — 25,414 food recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
About 7,400 units
Related Recalls
6
0 from same agency
Product description
The recalled supplement bottles are brown glass bottles that contain MegaFood One Daily Tablets. The bottles have a yellow label on the front with the words "MegaFood," "Fresh From Farm To Tablet," "One Daily," "Nourish," "Balance" and "Replenish" printed above a picture of vegetables. Recalled bottles have the following amounts, product codes and lot numbers: Amount Product Code Lot Numbers 60 tablets 51494 10151 10613, 10724 through 10728, 11246 and 12191 90 tablets 51494 10152 180 tablets 51494 10153 The amount is on the bottom right of the front label. The product code and lot numbers are on the left side of the front label.
Reason for recall
The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement tablets inside the bottle contain iron, which can cause serious injury or death to young children if multiple tablets are ingested at once.
Remedy — what to do
Consumers should immediately place bottles of this product out of reach of children and return any recalled bottles to the original place of purchase for a full refund or replacement.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 13110 |
| Date reported | January 31, 2013 |
| Date initiated | January 31, 2013 |
| Recalling firm | FoodState Inc., of Derry, N.h. |
| Affected scope | About 7,400 units |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately place bottles of this product out of reach of children and return any recalled bottles to the origin…
- Check the recall number (13110) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
The recalled supplement bottles are brown glass bottles that contain MegaFood One Daily Tablets. The bottles have a yellow label on the front with the words "MegaFood," "Fresh From Farm To Tablet," "One Daily," "Nourish," "Balance" and "Replenish" printed above a picture of vegetables. Recalled bottles have the following amounts, product codes and lot numbers: Amount Product Code Lot Numbers 60 tablets 51494 10151 10613, 10724 through 10728, 11246 and 12191 90 tablets 51494 10152 180 tablets 51494 10153 The amount is on the bottom right of the front label. The product code and lot numbers are on the left side of the front label.. Recalled by FoodState Inc., of Derry, N.h.. Units affected: About 7,400 units.
Why was this product recalled? ▼
The packaging is not child-resistant as required by the Poison Prevention Packaging Act. The supplement tablets inside the bottle contain iron, which can cause serious injury or death to young children if multiple tablets are ingested at once.
What should consumers do? ▼
Consumers should immediately place bottles of this product out of reach of children and return any recalled bottles to the original place of purchase for a full refund or replacement.
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 31, 2013. Severity: Moderate. Recall number: 13110.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (13110) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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What to do next
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Nearby Recalls in This Category
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported January 31, 2013.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
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.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.