Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported July 9, 2014
Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 50032 5
National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the front panel with 65 mg of elemental iron. The side panel and the tablets…
National Vitamin Co Inc recalled Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 5… - a moderate-severity action.
Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 5… was recalled by National Vitamin Co Inc in July 9, 2014. Reason: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the fro…. Check the official notice for the remedy. Verify recall #F-2061-2014 with the FDA Food before acting.
The recall
National Vitamin Co Inc issued this moderate-severity FDA Food recall-National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the fro….
- Moderate
- severity level
- 13K units
- affected scope
- Class II
- classification
- July 9, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2061-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2061-2014) was formally reported on July 9, 2014, with the manufacturer initiating the action on June 4, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. National Vitamin Co Inc is listed as the recalling firm, operating out of Casa Grande, AZ. Federal records list the affected scope as 13,240 units.
The documented reason for this recall is: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the front panel with 65 mg of elemental iron. The side panel and the tablets inside the bottle have the correct labe… Distribution data in the federal record shows the product reached: Nationwide in US. 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, 1 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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 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
13,240 units
Related Recalls
6
1 from same agency
Product description
Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 50032 5
Reason for recall
National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the front panel with 65 mg of elemental iron. The side panel and the tablets inside the bottle have the correct label with 36mg of elemental iron per tablet.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2061-2014 |
| Date reported | July 9, 2014 |
| Date initiated | June 4, 2014 |
| Recalling firm | National Vitamin Co Inc |
| Firm location | Casa Grande, AZ |
| Affected scope | 13,240 units |
| Distribution | Nationwide in US |
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.
- Check the recall number (F-2061-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 50032 5. Recalled by National Vitamin Co Inc. Units affected: 13,240 units.
Why was this product recalled? ▼
National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets because they are mislabeled on the front panel with 65 mg of elemental iron. The side panel and the tablets inside the bottle have the correct label with 36mg of elemental iron per tablet.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 9, 2014. Severity: Moderate. Recall number: F-2061-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide in US.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2061-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 July 9, 2014. 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.