Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported February 19, 2014
Bolt: Fat Incenerator capsules packaged within a container (60 capsules per bottle).
Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known as 1,3-dimethylamylamine, methylhexanamine or geranium extract in thei…
Mira Health Products Ltd. recalled Bolt: Fat Incenerator capsules packaged within a container (60 capsules per bottle). - a moderate-severity action.
Bolt: Fat Incenerator capsules packaged within a container (60 capsules per bottle). was recalled by Mira Health Products Ltd. in February 19, 2014. Reason: Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known …. Check the official notice for the remedy. Verify recall #F-1473-2014 with the FDA Food before acting.
The recall
Mira Health Products Ltd. issued this moderate-severity FDA Food recall-Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known ….
- Moderate
- severity level
- Class II
- classification
- February 19, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1473-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1473-2014) was formally reported on February 19, 2014, with the manufacturer initiating the action on July 23, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Mira Health Products Ltd. is listed as the recalling firm, operating out of Farmingdale, NY. Federal records list the affected scope as unknown (firm did not maintain accurate consistent logs).
The documented reason for this recall is: Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known as 1,3-dimethylamylamine, methylhexanamine or geranium extract in their raw materials. Distribution data in the federal record shows the product reached: GA. 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 - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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
unknown (firm did not maintain accurate consistent logs)
Related Recalls
6
0 from same agency
Product description
Bolt: Fat Incenerator capsules packaged within a container (60 capsules per bottle).
Reason for recall
Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known as 1,3-dimethylamylamine, methylhexanamine or geranium extract in their raw materials.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1473-2014 |
| Date reported | February 19, 2014 |
| Date initiated | July 23, 2013 |
| Recalling firm | Mira Health Products Ltd. |
| Firm location | Farmingdale, NY |
| Affected scope | unknown (firm did not maintain accurate consistent logs) |
| Distribution | GA |
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-1473-2014) 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? ▼
Bolt: Fat Incenerator capsules packaged within a container (60 capsules per bottle).. Recalled by Mira Health Products Ltd.. Units affected: unknown (firm did not maintain accurate consistent logs).
Why was this product recalled? ▼
Mira Health Products Ltd. recalled products marked as Dietary Supplements due to the use of DMAA, also known as 1,3-dimethylamylamine, methylhexanamine or geranium extract in their raw materials.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on February 19, 2014. Severity: Moderate. Recall number: F-1473-2014.
Where was the recalled product distributed? ▼
Distribution: GA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1473-2014) 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.
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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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 February 19, 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.